Canonical Allele Identifier: PA2579913053
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala256Val
CA346732415
NM_000251.3:c.767C>T