Canonical Allele Identifier: PA2573317565
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439100
ClinVar RCV Id: RCV001958029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Ser482Ala
CA358950819
NM_207352.4:c.1444T>G