Allele Registry

Canonical Allele Identifier: PA2828705449

Gene: ABCC9 HGNC NCBI

ClinVar Allele:

188838

ClinVar RCV:

RCV000171207

ClinVar Variation:

191032

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.His1174Tyr	CA235865 NM_001377273.1:c.3520C>T