Canonical Allele Identifier: PA2829621891
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 420904
ClinVar RCV Id: RCV000480387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Leu1219Arg
CA16619501
NM_005691.3:c.3656T>G