Canonical Allele Identifier: PA101715
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Asn423Tyr
CA119017
NM_000104.4:c.1267A>T