Canonical Allele Identifier: PA2826202762
Gene: TFG HGNC NCBI

Linked Data

ClinVar Variation Id: 466412
ClinVar RCV Id: RCV001755843 RCV000554884 RCV002384150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182408.1:p.Thr326Ala
CA2517240
NM_001195479.2:c.976A>G