Canonical Allele Identifier: PA106816
Gene: CYP2U1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39501
ClinVar RCV Id: RCV000032697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898898.1:p.Glu380Gly
CA130342
NM_183075.3:c.1139A>G