Canonical Allele Identifier: PA106787
Gene: CYP2U1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39504
ClinVar RCV Id: RCV000032700 RCV000814689 RCV001847627 RCV002264909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898898.1:p.Arg488Trp
CA130344
NM_183075.3:c.1462C>T