ClinGen Allele Registry
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Canonical Allele Identifier:
PA891852281
Gene: TARDBP
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0588428076
Linked Data - NCBI & NCI
ClinVar Allele:
576388
ClinVar RCV:
RCV000713826
ClinVar Variation:
586812
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_031401.1:p.Gly298Cys
CA338364694
NM_007375.4:c.892G>T