Canonical Allele Identifier: PA645468369
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 335951
ClinVar RCV Id: RCV000292895 RCV000347501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.His401Arg
CA10615175
NM_000104.4:c.1202A>G