Canonical Allele Identifier: PA1139736701
Gene: TARDBP HGNC NCBI

Linked Data

ClinVar Variation Id: 941988
ClinVar RCV Id: RCV001211878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031401.1:p.Asn70Asp
CA338356403
NM_007375.4:c.208A>G