Canonical Allele Identifier: PA1139766133
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 972481
ClinVar RCV Id: RCV001248522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Arg525Ser
CA3162896
NM_207352.4:c.1573C>A