Canonical Allele Identifier: PA2829425317
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 3176628
ClinVar RCV Id: RCV004474488
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ala2729Thr
CA186356980
NM_003235.5:c.8185G>A