Canonical Allele Identifier: PA2826465715
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838884
ClinVar RCV Id: RCV001040531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala782Val
CA346730846
NM_001258281.1:c.2345C>T