Allele Registry

Canonical Allele Identifier: PA235878

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000171209

RCV001050168

RCV002415726

RCV002478542

ClinVar Variation:

191034

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Arg660Trp	CA235875 NM_005691.3:c.1978C>T