Allele Registry

Canonical Allele Identifier: PA122351

Gene: TNF HGNC NCBI

ClinVar RCV:

RCV000013187

ClinVar Variation:

12386

HGVS (amino-acid)	Matching Registered Transcripts
NP_000585.2:p.Arg108Trp	CA122350 NM_000594.4:c.322C>T