Canonical Allele Identifier: PA162447
Gene: TNFRSF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 135349
ClinVar RCV Id: RCV000122164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003811.2:p.Lys17Arg
CA162445
NM_003820.3:c.50A>G