Allele Registry

Canonical Allele Identifier: PA2573074292

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029190

ClinVar Variation:

35535

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364203.1:p.Ser731Pro	CA260091 NM_001377274.1:c.2191T>C