Canonical Allele Identifier: PA101978
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 225333
ClinVar RCV Id: RCV000312523 RCV000490426 RCV002485372 RCV003758726 RCV003488467
ClinVar Variation Id: 2988516
ClinVar RCV Id: RCV003846683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000095.2:p.Val320Leu
CA1619915
NM_000104.4:c.958G>T
CA45510259
NM_000104.4:c.958G>C