Canonical Allele Identifier: PA101903
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1254629
ClinVar RCV Id: RCV001658811 RCV003470876 RCV003594146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Pro437Leu
CA1619819
NM_000104.4:c.1310C>T