Canonical Allele Identifier: PA101778
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7735
ClinVar RCV Id: RCV000008174 RCV000724653 RCV000791358 RCV001201386 RCV001375550 RCV002490338 RCV003466834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Glu387Lys
CA254241
NM_000104.4:c.1159G>A