Canonical Allele Identifier: PA2499305844
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046129
ClinVar RCV Id: RCV001350644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Arg452Cys
CA3162839
NM_207352.4:c.1354C>T