Canonical Allele Identifier: PA645506992
Gene: TFG HGNC NCBI

Linked Data

ClinVar Variation Id: 245772
ClinVar RCV Id: RCV000235479 RCV000533138 RCV001081716 RCV002411066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006061.2:p.Pro354Ala
CA2517248
NM_006070.6:c.1060C>G