Allele Registry

Canonical Allele Identifier: PA645472022

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000222095

RCV000526634

RCV000757937

ClinVar Variation:

231904

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ser255Gly	CA040330 NM_000251.3:c.763A>G