Canonical Allele Identifier: PA162446
Gene: TNFRSF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 135349
ClinVar RCV Id: RCV000122164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284534.1:p.Lys17Arg
CA162445
NM_001297605.2:c.50A>G