Canonical Allele Identifier: PA101755
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1329081
ClinVar RCV Id: RCV001797972 RCV002489845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Gln144Arg
CA1620036
NM_000104.4:c.431A>G