Allele Registry

Canonical Allele Identifier: PA105708

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029190

ClinVar Variation:

35535

HGVS (amino-acid)	Matching Registered Transcripts
NP_005682.2:p.Ser1020Pro	CA260091 NM_005691.3:c.3058T>C