Allele Registry

Canonical Allele Identifier: PA105616

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029188

RCV001216671

ClinVar Variation:

35533

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Arg1116His	CA260083 NM_005691.3:c.3347G>A