Canonical Allele Identifier: PA658673018
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln793Arg
CA346730091
NM_000251.3:c.2378A>G