Canonical Allele Identifier: PA658804046
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala604Thr
CA346728336
NM_000251.3:c.1810G>A