Allele Registry

Canonical Allele Identifier: PA331721

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076775

RCV001554291

RCV003593904

ClinVar Variation:

91270

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu330Pro	CA022706 NM_000251.3:c.989T>C