ClinGen Allele Registry
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Canonical Allele Identifier:
PA113382
Gene: TARDBP
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.0064747307
Linked Data - NCBI & NCI
ClinVar Allele:
20267
ClinVar RCV:
RCV000005539
RCV000693006
RCV001090806
ClinVar Variation:
5228
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_031401.1:p.Met337Val
CA340373
NM_007375.4:c.1009A>G