Canonical Allele Identifier: PA645376659
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348311
ClinVar RCV Id: RCV000298644 RCV000355789 RCV001055970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Pro430Leu
CA3162819
NM_207352.4:c.1289C>T