Canonical Allele Identifier: PA097150
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 976233
ClinVar RCV Id: RCV001253461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000065.1:p.Trp140Arg
CA414755568
NM_000074.3:c.418T>A
CA414755569
NM_000074.3:c.418T>C