Canonical Allele Identifier: PA276933
Gene: CYP4V2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Asn466Asp
CA276932
NM_207352.4:c.1396A>G