Canonical Allele Identifier: PA113382
Gene: TARDBP HGNC NCBI

Linked Data

ClinVar Variation Id: 5228
ClinVar RCV Id: RCV000005539 RCV000693006 RCV001090806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031401.1:p.Met337Val
CA340373
NM_007375.4:c.1009A>G