Canonical Allele Identifier: PA113232
Gene: TARDBP HGNC NCBI

Linked Data

ClinVar Variation Id: 21482
ClinVar RCV Id: RCV000020671 RCV001851977 RCV002051795 RCV003242964 RCV003904854 RCV004546414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031401.1:p.Asn267Ser
CA586454
NM_007375.4:c.800A>G