Canonical Allele Identifier: PA2499263572
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 1176276
ClinVar RCV Id: RCV001531719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Arg170del
CA2579253657
NM_003235.5:c.509_511del