Canonical Allele Identifier: PA2741922268
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2625271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Ser1520Tyr
CA384129336
NM_005691.3:c.4559C>A