Canonical Allele Identifier: PA280829
Gene: TNFRSF1A HGNC NCBI

Linked Data

ClinVar Variation Id: 97690
ClinVar RCV Id: RCV000083943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001056.1:p.Cys102Trp
CA280827
NM_001065.4:c.306C>G