Canonical Allele Identifier: PA299401
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln264Arg
CA022268
NM_000251.3:c.791A>G