Canonical Allele Identifier: PA2579922574
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719177
ClinVar RCV Id: RCV002301937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp823Val
CA346730549
NM_000251.3:c.2468A>T