Allele Registry

Canonical Allele Identifier: PA2829620865

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000441926

ClinVar Variation:

383474

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Asp793Val	CA16607204 NM_005691.3:c.2378A>T