Allele Registry

Canonical Allele Identifier: PA2826682961

Gene: ICOSLG HGNC NCBI

ClinVar RCV:

RCV001824255

ClinVar Variation:

1339546

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269980.1:p.Pro50Ser	CA410615090 NM_001283051.2:c.148C>T