Canonical Allele Identifier: PA111258
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39249
ClinVar RCV Id: RCV000032526
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Ser341Pro
CA343705
NM_207352.4:c.1021T>C