Canonical Allele Identifier: PA2825069550
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3079388
ClinVar RCV Id: RCV004367782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Ser485Pro
CA346327124
NM_000104.4:c.1453T>C