Allele Registry

Canonical Allele Identifier: PA2826682861

Gene: ICOSLG HGNC NCBI

ClinVar RCV:

RCV001824255

ClinVar Variation:

1339546

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269979.1:p.Pro167Ser	CA410615090 NM_001283050.2:c.499C>T