Allele Registry

Canonical Allele Identifier: PA2828704702

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029191

ClinVar Variation:

35536

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.His60Tyr	CA260095 NM_001377273.1:c.178C>T