Canonical Allele Identifier: PA331681
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met261Thr
CA022248
NM_000251.3:c.782T>C