Canonical Allele Identifier: PA101962
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7744
ClinVar RCV Id: RCV000008185 RCV000059337 RCV000078126 RCV000766838 RCV001087298 RCV001139671 RCV001139670 RCV002470703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Tyr81Asn
CA145182
NM_000104.4:c.241T>A