Canonical Allele Identifier: PA2573218436
Gene: TNFRSF9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1363542
ClinVar RCV Id: RCV001934944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001552.2:p.Val156Met
CA338158553
NM_001561.6:c.466G>A