Allele Registry

Canonical Allele Identifier: PA2580102169

Gene: CD40LG HGNC NCBI

ClinVar Variation Id: 1701614

ClinVar RCV Id: RCV002276236

ClinVar Variation Id: 2431549

ClinVar RCV Id: RCV003140603

HGVS (amino-acid)	Matching Registered Transcripts
NP_000065.1:p.Phe229Leu	CA414756513 NM_000074.3:c.685T>C CA414756532 NM_000074.3:c.687T>A CA414756535 NM_000074.3:c.687T>G