ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA658820577
Gene: TARDBP
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0313840281
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000020657
RCV000993301
RCV001851975
ClinVar Variation:
21468
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_031401.1:p.Asn352Ser
CA17876354
NM_007375.4:c.1055A>G