ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA294050
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.35698504
Score
0.4814320368
Score
-0.4741526241
Score
0.5793028413
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000129457
RCV000213049
RCV000696142
RCV000785522
RCV004019730
ClinVar Variation:
141098
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Lys120Glu
CA000130
NM_000546.6:c.358A>G