ClinGen Allele Registry
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Canonical Allele Identifier:
PA276933
Gene: CYP4V2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
206572
ClinVar RCV:
RCV000191926
ClinVar Variation:
209986
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_997235.3:p.Asn466Asp
CA276932
NM_207352.4:c.1396A>G