Canonical Allele Identifier: PA101635
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7739
ClinVar RCV Id: RCV000008178 RCV000023146 RCV000059335 RCV000489962 RCV000709869 RCV000778148 RCV000844695 RCV001083921 RCV001258308 RCV003466835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Arg368His
CA119016
NM_000104.4:c.1103G>A