Canonical Allele Identifier: PA2573317472
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1355601
ClinVar RCV Id: RCV001888081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Asn104Asp
CA3162495
NM_207352.4:c.310A>G