Canonical Allele Identifier: PA2573317568
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1487320
ClinVar RCV Id: RCV002006370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Arg519Ser
CA358951372
NM_207352.4:c.1557G>C
CA358951374
NM_207352.4:c.1557G>T