Canonical Allele Identifier: PA1139766119
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 954493
ClinVar RCV Id: RCV001226952 RCV002563105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Arg525Cys
CA3162897
NM_207352.4:c.1573C>T