Canonical Allele Identifier: PA2741885579
Gene: TNFRSF9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2790765
ClinVar RCV Id: RCV003670075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001552.2:p.Gly131Ile
CA2739272242
NM_001561.6:c.391_392delinsAT