Canonical Allele Identifier: PA2826202513
Gene: TFG HGNC NCBI

Linked Data

ClinVar Variation Id: 466404
ClinVar RCV Id: RCV000558585 RCV001644651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182407.1:p.Thr364Pro
CA2517252
NM_001195478.2:c.1090A>C