Allele Registry

Canonical Allele Identifier: PA2826465094

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000823002

RCV002415942

RCV003467514

RCV004002849

ClinVar Variation:

664827

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Met622Thr	CA346729169 NM_001258281.1:c.1865T>C