Canonical Allele Identifier: PA2499230091
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly827Glu
CA346730603
NM_000251.3:c.2480G>A