Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-10-16T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
This migration is underway but taking longer than originally estimated.

Canonical Allele Identifier: PA2826463236

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219839

ClinVar RCV Id: RCV001346084

ClinVar Variation Id: 423759

ClinVar RCV Id: RCV000481717 RCV001178629 RCV001865483

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu179Phe	CA348622 NM_001258281.1:c.537G>C CA16617561 NM_001258281.1:c.537G>T