Allele Registry

Canonical Allele Identifier: PA645500122

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000241944

RCV000280505

RCV003669121

ClinVar Variation:

258993

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Asp1312Gly	CA4883953 NM_003235.5:c.3935A>G