Allele Registry

Canonical Allele Identifier: PA2828705182

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000441926

ClinVar Variation:

383474

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.Asp793Val	CA16607204 NM_001377273.1:c.2378A>T