Canonical Allele Identifier: PA101769
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 68467
ClinVar RCV Id: RCV000059338 RCV000175523 RCV000761427 RCV000986620 RCV001804801 RCV001513104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Glu229Lys
CA145183
NM_000104.4:c.685G>A