Canonical Allele Identifier: PA112777
Gene: TFG HGNC NCBI

Linked Data

ClinVar Variation Id: 37089
ClinVar RCV Id: RCV000030736 RCV000218755 RCV000642397 RCV001095428 RCV002251934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007566.1:p.Pro285Leu
CA130077
NM_001007565.2:c.854C>T