Canonical Allele Identifier: PA1139736701
Gene: TARDBP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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