Canonical Allele Identifier: PA119013
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7736
ClinVar RCV Id: RCV000008175 RCV003155022 RCV003593856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Met1Thr