ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579936473
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.43095762
Score
1.2608274458
Score
-1.3159331515
Score
-0.085636899
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000572692
RCV001352113
RCV002289793
ClinVar Variation:
480751
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gln136Glu
CA397842769
NM_000546.6:c.406C>G