Allele Registry

Canonical Allele Identifier: PA101666

Gene: CYP1B1 HGNC NCBI

ClinVar Variation Id: 2203048

HGVS (amino-acid)	Matching Registered Transcripts
NP_000095.2:p.Arg390Ser	CA1619848 NM_000104.4:c.1168C>A