Canonical Allele Identifier: PA2580102159
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 2228477
ClinVar RCV Id: RCV002707708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000065.1:p.Arg181Trp
CA10528154
NM_000074.3:c.541C>T