Canonical Allele Identifier: PA645376704
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Met475Val
CA3162860
NM_207352.4:c.1423A>G