Canonical Allele Identifier: PA2826202778
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_001182408.1:p.Pro350Ala
CA2517248
NM_001195479.2:c.1048C>G