Canonical Allele Identifier: PA113293
Gene: TARDBP HGNC NCBI

Linked Data

ClinVar Variation Id: 21483
ClinVar RCV Id: RCV000020672 RCV000412864 RCV000529539 RCV000492328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031401.1:p.Gly287Ser
CA586459
NM_007375.4:c.859G>A