Canonical Allele Identifier: PA275486
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 202204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly820Asp
CA020624
NM_000251.3:c.2459G>A