Canonical Allele Identifier: PA343715
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39254
ClinVar RCV Id: RCV000032531 RCV000659009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Arg400His
CA343714
NM_207352.4:c.1199G>A