Allele Registry

Canonical Allele Identifier: PA105658

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000024626

ClinVar Variation:

31948

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Cys1043Tyr	CA260066 NM_005691.3:c.3128G>A