Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
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This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.

Canonical Allele Identifier: PA645383766

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 421360

ClinVar RCV Id: RCV000478043 RCV002323830 RCV002526597

ClinVar Variation Id: 479972

ClinVar RCV Id: RCV000565899 RCV001858114 RCV003459294

ClinVar Variation Id: 1729541

ClinVar RCV Id: RCV002324974

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe1088Leu	CA16617695 NM_000179.3:c.3262T>C CA346758166 NM_000179.3:c.3264C>A CA346758170 NM_000179.3:c.3264C>G CA2580067019 NM_000179.3:c.3262_3264delinsCTT