Allele Registry

Canonical Allele Identifier: PA2828184163

Gene: ICOSLG HGNC NCBI

ClinVar RCV:

RCV001824255

ClinVar Variation:

1339546

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352688.1:p.Pro140Ser	CA410615090 NM_001365759.2:c.418C>T