Canonical Allele Identifier: PA1139765968
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 960507
ClinVar RCV Id: RCV001234046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Arg225Thr
CA358947844
NM_207352.4:c.674G>C