Canonical Allele Identifier: PA260208
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 35813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000065.1:p.Gly219Arg
CA260206
NM_000074.3:c.655G>A
CA414756340
NM_000074.3:c.655G>C