Canonical Allele Identifier: PA2580570967
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1940989
ClinVar RCV Id: RCV002675510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Val408Leu
CA3162789
NM_207352.4:c.1222G>T
CA358950325
NM_207352.4:c.1222G>C