Allele Registry

Canonical Allele Identifier: PA2826463336

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001027097

RCV001358282

RCV002230810

RCV003470449

ClinVar Variation:

408531

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser202Leu	CA040677 NM_001258281.1:c.605C>T