Canonical Allele Identifier: PA136259
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 45400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Ala717Thr
CA136256
NM_005691.3:c.2149G>A