Allele Registry

Canonical Allele Identifier: PA1139704279

Gene: TG HGNC NCBI

ClinVar Variation Id: 912286

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Asp2001Asn	CA4884725 NM_003235.5:c.6001G>A