Allele Registry

Canonical Allele Identifier: PA915984139

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000693598

RCV003584715

RCV003999599

ClinVar Variation:

572259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn61Thr	CA346730352 NM_001258281.1:c.182A>C