Canonical Allele Identifier: PA1139765984
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 950810
ClinVar RCV Id: RCV001222607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Glu250del
CA557053842
NM_207352.4:c.749_751del