Canonical Allele Identifier: PA113268
Gene: TARDBP HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031401.1:p.Asp169Gly
CA340377
NM_007375.4:c.506A>G