Allele Registry

Canonical Allele Identifier: PA2828705432

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000254900

ClinVar Variation:

265666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.Arg1154Gly	CA10588545 NM_001377273.1:c.3460C>G