Canonical Allele Identifier: PA915961557
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 744901
ClinVar RCV Id: RCV000921393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000065.1:p.Phe201Leu
CA10528164
NM_000074.3:c.601T>C
CA414756048
NM_000074.3:c.603C>A
CA414756051
NM_000074.3:c.603C>G