Allele Registry

Canonical Allele Identifier: PA164986

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000129729

RCV000460057

RCV000588274

RCV000761179

RCV002267870

ClinVar Variation:

141281

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile454Val	CA018091 NM_000251.3:c.1360A>G