Canonical Allele Identifier: PA2826202553
Gene: TFG HGNC NCBI

Linked Data

ClinVar Variation Id: 432643
ClinVar RCV Id: RCV000497384
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182408.1:p.Ser8Arg
CA353836672
NM_001195479.2:c.22A>C
CA353836678
NM_001195479.2:c.24T>A
CA353836679
NM_001195479.2:c.24T>G