Allele Registry

Canonical Allele Identifier: PA2828704963

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000024627

ClinVar Variation:

31949

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364202.1:p.Ala478Val	CA260070 NM_001377273.1:c.1433C>T