Allele Registry

Canonical Allele Identifier: PA2828705408

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029188

RCV001216671

ClinVar Variation:

35533

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.Arg1116His	CA260083 NM_001377273.1:c.3347G>A