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: PA190787

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185016

ClinVar RCV Id: RCV000164368 RCV000985840

ClinVar Variation Id: 628563

ClinVar RCV Id: RCV000773055 RCV002534049

ClinVar Variation Id: 1797436

ClinVar RCV Id: RCV002438061 RCV003594302

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe10Leu	CA011525 NM_000179.3:c.30C>G CA069791 NM_000179.3:c.28T>C CA346734516 NM_000179.3:c.30C>A