Allele Registry

Canonical Allele Identifier: PA2826463177

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000129911

RCV000465942

RCV001551502

RCV003460906

RCV003997535

ClinVar Variation:

141406

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser167Cys	CA022041 NM_001258281.1:c.500C>G