Allele Registry

Canonical Allele Identifier: PA196052

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000166506

RCV000629905

RCV001355772

RCV003477630

RCV003995508

ClinVar Variation:

186853

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys471Asn	CA018242 NM_000251.3:c.1413A>C CA346726778 NM_000251.3:c.1413A>T