Canonical Allele Identifier: PA2580103129
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1701377
ClinVar RCV Id: RCV002276073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Arg368Ile
CA2580066422
NM_000104.4:c.1102_1104delinsATC