Allele Registry

Canonical Allele Identifier: PA2829621741

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV001901407

ClinVar Variation:

1403970

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Arg1154Pro	CA6481113 NM_005691.3:c.3461G>C