Allele Registry

Canonical Allele Identifier: PA658820277

Gene: CYP7B1 HGNC NCBI

ClinVar Variation Id: 500781

HGVS (amino-acid)	Matching Registered Transcripts
NP_004811.1:p.Ala32Ser	CA4764306 NM_004820.5:c.94G>T