Allele Registry

Canonical Allele Identifier: PA2829621743

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000254900

ClinVar Variation:

265666

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Arg1154Gly	CA10588545 NM_005691.3:c.3460C>G