Canonical Allele Identifier: PA891844608
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 571519
ClinVar RCV Id: RCV000692689
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro472Ala
CA346726782
NM_000251.3:c.1414C>G