Allele Registry

Canonical Allele Identifier: PA2828705410

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000426515

ClinVar Variation:

387946

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.Arg1116Leu	CA16607192 NM_001377273.1:c.3347G>T