Canonical Allele Identifier: PA2580570946
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715573
ClinVar RCV Id: RCV002301333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Met247Leu
CA358948010
NM_207352.4:c.739A>T
CA358948011
NM_207352.4:c.739A>C