Canonical Allele Identifier: PA097161
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 2138729
ClinVar RCV Id: RCV003066383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000065.1:p.Trp140Cys
CA414755572
NM_000074.3:c.420G>T
CA414755573
NM_000074.3:c.420G>C