Allele Registry

Canonical Allele Identifier: PA2829620327

Gene: ABCC9 HGNC NCBI

ClinVar Allele:

408618

ClinVar RCV:

RCV000486887

ClinVar Variation:

421386

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Val462Ala	CA16619503 NM_005691.3:c.1385T>C