Canonical Allele Identifier: PA106797
Gene: CYP2U1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39500
ClinVar RCV Id: RCV000032696 RCV000162142 RCV000162185 RCV000442087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898898.1:p.Asp316Val
CA130341
NM_183075.3:c.947A>T