Canonical Allele Identifier: PA149665
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39267
ClinVar RCV Id: RCV000032544 RCV000082840 RCV000132719 RCV000278726 RCV003887878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Leu22Val
CA149664
NM_207352.4:c.64C>G