ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA170882
Gene: TFG
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000144505
ClinVar Variation:
156445
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001007566.1:p.Gly269Val
CA170881
NM_001007565.2:c.806G>T