Canonical Allele Identifier: PA2580318981
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717039
ClinVar RCV Id: RCV002297405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Gly1522Ser
CA384129301
NM_005691.3:c.4564G>A