Allele Registry

Canonical Allele Identifier: PA2826463593

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076775

RCV001554291

RCV003593904

ClinVar Variation:

91270

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu264Pro	CA022706 NM_001258281.1:c.791T>C