Canonical Allele Identifier: PA658813642
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 497287
ClinVar RCV Id: RCV000594902 RCV001150364 RCV001150365 RCV001429168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Arg443Gln
CA3162830
NM_207352.4:c.1328G>A