Canonical Allele Identifier: PA101645
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 335952
ClinVar RCV Id: RCV000307738 RCV000396035 RCV001782854 RCV002230703 RCV003470319 RCV003593949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Arg390Cys
CA1619847
NM_000104.4:c.1168C>T