Allele Registry

Canonical Allele Identifier: PA2828705487

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000480387

ClinVar Variation:

420904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.Leu1219Arg	CA16619501 NM_001377273.1:c.3656T>G