Canonical Allele Identifier: PA916019712
Gene: TGDS HGNC NCBI

Linked Data

ClinVar Variation Id: 162455
ClinVar RCV Id: RCV000149817 RCV000624586 RCV001092080 RCV003415988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291359.1:p.Ala68Ser
CA175045
NM_001304430.2:c.202G>T