Canonical Allele Identifier: PA2579913114
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760664
ClinVar RCV Id: RCV002409883
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu260Val
CA346732467
NM_000251.3:c.779A>T