Canonical Allele Identifier: PA645461694
Gene: CYP2U1 HGNC NCBI

Linked Data

ClinVar Variation Id: 433182
ClinVar RCV Id: RCV000498760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898898.1:p.Pro151Leu
CA357833324
NM_183075.3:c.452C>T