Allele Registry

Canonical Allele Identifier: PA101805

Gene: CYP1B1 HGNC NCBI

ClinVar Allele:

22771

ClinVar RCV:

RCV000008171

ClinVar Variation:

7732

HGVS (amino-acid)	Matching Registered Transcripts
NP_000095.2:p.Gly365Trp	CA254238 NM_000104.4:c.1093G>T