Canonical Allele Identifier: PA2579918528
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779285
ClinVar RCV Id: RCV002401484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val582Asp
CA346728211
NM_000251.3:c.1745T>A