Canonical Allele Identifier: PA645499941
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 436996
ClinVar RCV Id: RCV000501874 RCV000760170 RCV000764740 RCV001729618 RCV003155217
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Gly77Ser
CA4882834
NM_003235.5:c.229G>A