Allele Registry

Canonical Allele Identifier: PA645500237

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000242253

RCV000305066

RCV001651176

ClinVar Variation:

258996

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Asp1838Asn	CA4884537 NM_003235.5:c.5512G>A