ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA113338
Gene: TARDBP
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.1439853691
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000020674
RCV003764615
ClinVar Variation:
21485
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_031401.1:p.Gly295Ser
CA342123
NM_007375.4:c.883G>A