Allele Registry

Canonical Allele Identifier: PA2828705641

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000008640

ClinVar Variation:

8162

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.Ala1513Thr	CA254332 NM_001377273.1:c.4537G>A