Canonical Allele Identifier: PA2579918529
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779287
ClinVar RCV Id: RCV002401486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val582Ala
CA346728212
NM_000251.3:c.1745T>C