ClinGen Allele Registry
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Canonical Allele Identifier:
PA129039
Gene: CYP1B1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000023148
RCV000349391
RCV001139674
RCV001139675
RCV003155038
ClinVar Variation:
30224
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000095.2:p.Pro52Leu
CA129038
NM_000104.4:c.155C>T