Allele Registry

Canonical Allele Identifier: PA109644

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000013541

RCV002273929

ClinVar Variation:

12704

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Cys1897Tyr	CA210710 NM_003235.5:c.5690G>A