Canonical Allele Identifier: PA2826463198
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 640478
ClinVar RCV Id: RCV000793508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr172Phe
CA346732076
NM_001258281.1:c.515A>T