Canonical Allele Identifier: PA645376476
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348300
ClinVar RCV Id: RCV000309066 RCV000358766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997235.3:p.Asn104Ser
CA10620604
NM_207352.4:c.311A>G