Canonical Allele Identifier: PA113338
Gene: TARDBP HGNC NCBI

Linked Data

ClinVar Variation Id: 21485
ClinVar RCV Id: RCV000020674 RCV003764615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031401.1:p.Gly295Ser
CA342123
NM_007375.4:c.883G>A