Canonical Allele Identifier: PA913191343
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 624445
ClinVar RCV Id: RCV000762673 RCV003512077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000065.1:p.Phe229Ser
CA414756523
NM_000074.3:c.686T>C