Canonical Allele Identifier: PA236986
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 191585
ClinVar RCV Id: RCV000171851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Thr1100Ile
CA236983
NM_005691.3:c.3299C>T