Allele Registry

Canonical Allele Identifier: PA199988

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029274

RCV000038600

RCV000172738

RCV000251925

RCV000852670

RCV001082826

RCV001528354

ClinVar Variation:

35627

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Val734Ile	CA199985 NM_005691.3:c.2200G>A