Canonical Allele Identifier: PA2579913843
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp303Gly
CA346732958
NM_000251.3:c.908A>G