Canonical Allele Identifier: PA2829621622
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 969387
ClinVar RCV Id: RCV001244724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Leu1093Val
CA384118142
NM_005691.3:c.3277C>G