Canonical Allele Identifier: PA101606
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2503881
ClinVar RCV Id: RCV003230872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Ala115Pro
CA1620052
NM_000104.4:c.343G>C