Allele Registry

Canonical Allele Identifier: PA645500000

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000388671

RCV003688850

RCV004555558

ClinVar Variation:

361924

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Gly815Arg	CA4883405 NM_003235.5:c.2443G>A CA372235984 NM_003235.5:c.2443G>C