ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936766
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.443095024
Score
-0.187834983
Score
-2.720037576
Score
0.1869526486
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000537102
RCV001177908
RCV001821513
RCV002289729
ClinVar Variation:
458536
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu114Ser
CA002835
NM_000546.6:c.341T>C