Allele Registry

Canonical Allele Identifier: PA915984341

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000221949

RCV001365859

RCV003997762

ClinVar Variation:

229726

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val97Ala	CA10577939 NM_001258281.1:c.290T>C