Allele Registry

Canonical Allele Identifier: PA210697

Gene: TG HGNC NCBI

ClinVar Allele:

27729

ClinVar RCV:

RCV000013527

RCV000880032

RCV001002732

ClinVar Variation:

12690

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Gln870His	CA210696 NM_003235.5:c.2610G>T CA372236882 NM_003235.5:c.2610G>C