Allele Registry

Canonical Allele Identifier: PA2826462719

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000195508

RCV000581797

RCV001770148

RCV003114359

RCV003997016

ClinVar Variation:

216347

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Met1Val