Allele Registry

Canonical Allele Identifier: PA101796

Gene: CYP1B1 HGNC NCBI

ClinVar RCV:

RCV000008179

RCV003843390

ClinVar Variation:

7740

2984231

HGVS (amino-acid)	Matching Registered Transcripts
NP_000095.2:p.Gly232Arg	CA254242 NM_000104.4:c.694G>C CA346328704 NM_000104.4:c.694G>A