Allele Registry

Canonical Allele Identifier: PA2828705358

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000024626

ClinVar Variation:

31948

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.Cys1043Tyr	CA260066 NM_001377273.1:c.3128G>A