Allele Registry

Canonical Allele Identifier: PA260086

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029188

RCV001216671

ClinVar Variation:

35533

HGVS (amino-acid)	Matching Registered Transcripts
NP_064693.2:p.Arg1116His	CA260083 NM_020297.3:c.3347G>A