Canonical Allele Identifier: PA2580570965
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119167
ClinVar RCV Id: RCV003054527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Cys406Tyr
CA112134823
NM_207352.4:c.1217G>A