Canonical Allele Identifier: PA101685
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7733
ClinVar RCV Id: RCV000008172 RCV000255845 RCV003466833 RCV003155021 RCV002512894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Arg469Trp
CA254239
NM_000104.4:c.1405C>T