Canonical Allele Identifier: PA1139766059
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 972198
ClinVar RCV Id: RCV001248173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Asp356Val
CA112131673
NM_207352.4:c.1067A>T