Canonical Allele Identifier: PA1139736799
Gene: TARDBP HGNC NCBI

Linked Data

ClinVar Variation Id: 939152
ClinVar RCV Id: RCV001208497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031401.1:p.Asn378Asp
CA338368255
NM_007375.4:c.1132A>G