Canonical Allele Identifier: PA2580570939
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087705
ClinVar RCV Id: RCV003000093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.His180Gln
CA358947525
NM_207352.4:c.540C>A
CA358947526
NM_207352.4:c.540C>G