Canonical Allele Identifier: PA2580103102
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2263895
ClinVar RCV Id: RCV002798254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Ala133Pro
CA1620041
NM_000104.4:c.397G>C