Canonical Allele Identifier: PA2826202342
Gene: TFG HGNC NCBI

Linked Data

ClinVar Variation Id: 100909
ClinVar RCV Id: RCV000087273 RCV002321583 RCV001038327 RCV001549766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182407.1:p.Arg106Cys
CA150664
NM_001195478.2:c.316C>T