Canonical Allele Identifier: PA658820577
Gene: TARDBP HGNC NCBI

Linked Data

ClinVar Variation Id: 21468
ClinVar RCV Id: RCV000020657 RCV000993301 RCV001851975
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031401.1:p.Asn352Ser
CA17876354
NM_007375.4:c.1055A>G