Canonical Allele Identifier: PA097077
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 569900
ClinVar RCV Id: RCV000690645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000065.1:p.Leu258Ser
CA414757172
NM_000074.3:c.773T>C