Canonical Allele Identifier: PA2579913147
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu262Lys
CA346732491
NM_000251.3:c.784G>A