Allele Registry

Canonical Allele Identifier: PA3057313041

Gene: CYP1B1 HGNC NCBI

ClinVar RCV:

RCV004795752

ClinVar Variation:

3382864

HGVS (amino-acid)	Matching Registered Transcripts
NP_000095.2:p.Gly365Arg	CA45506756 NM_000104.4:c.1093G>C CA346327872 NM_000104.4:c.1093G>A