Allele Registry

Canonical Allele Identifier: PA2828705838

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000171209

RCV001050168

RCV002415726

RCV002478542

ClinVar Variation:

191034

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364203.1:p.Arg372Trp	CA235875 NM_001377274.1:c.1114C>T