Allele Registry

Canonical Allele Identifier: PA210988

Gene: CYP7B1 HGNC NCBI

ClinVar Allele:

125787

ClinVar RCV:

RCV000106302

RCV000200232

RCV000422978

RCV003415876

ClinVar Variation:

120179

HGVS (amino-acid)	Matching Registered Transcripts
NP_004811.1:p.Thr297Ala	CA210987 NM_004820.5:c.889A>G