Canonical Allele Identifier: PA096995
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 11159
ClinVar RCV Id: RCV000011909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000065.1:p.Gly227Val
CA255745
NM_000074.3:c.680G>T