Canonical Allele Identifier: PA645475926
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408542
ClinVar RCV Id: RCV002230812 RCV003470450
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu853del
CA1649293
NM_000251.3:c.2557_2559del