Allele Registry

Canonical Allele Identifier: PA2829621657

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000426515

ClinVar Variation:

387946

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Arg1116Leu	CA16607192 NM_005691.3:c.3347G>T