Canonical Allele Identifier: PA101829
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7730
ClinVar RCV Id: RCV000008169 RCV000255452 RCV000763083 RCV001206715 RCV001335112 RCV003483427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Gly61Glu
CA254237
NM_000104.4:c.182G>A