Allele Registry

Canonical Allele Identifier: PA2828705719

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000486887

ClinVar Variation:

421386

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364203.1:p.Val174Ala	CA16619503 NM_001377274.1:c.521T>C