Canonical Allele Identifier: PA2573317562
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494755
ClinVar RCV Id: RCV001989577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Lys471Thr
CA3162858
NM_207352.4:c.1412A>C