Allele Registry

Canonical Allele Identifier: PA2828705726

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000024627

ClinVar Variation:

31949

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364203.1:p.Ala190Val	CA260070 NM_001377274.1:c.569C>T