Canonical Allele Identifier: PA2826463317
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1473785
ClinVar RCV Id: RCV001970864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn197Tyr
CA346732507
NM_001258281.1:c.589A>T