Allele Registry

Canonical Allele Identifier: PA2826464457

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000160593

RCV000773929

RCV000774571

RCV001067826

RCV002290018

RCV002401003

RCV003462090

RCV003998474

RCV004001338

ClinVar Variation:

182565

629230

1776525

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Phe473Leu	CA018746 NM_001258281.1:c.1419T>A CA346727924 NM_001258281.1:c.1417T>C CA346727929 NM_001258281.1:c.1419T>G