Canonical Allele Identifier: PA097169
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 11164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000065.1:p.Trp140Gly
CA255754
NM_000074.3:c.418T>G