Canonical Allele Identifier: PA2573317536
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353754
ClinVar RCV Id: RCV001863583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Ser394Phe
CA3162777
NM_207352.4:c.1181C>T