Canonical Allele Identifier: PA2825287895
Gene: TFG HGNC NCBI

Linked Data

ClinVar Variation Id: 432643
ClinVar RCV Id: RCV000497384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007566.1:p.Ser8Arg
CA353836672
NM_001007565.2:c.22A>C
CA353836678
NM_001007565.2:c.24T>A
CA353836679
NM_001007565.2:c.24T>G