ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA193948
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.8526733318
Score
-2.223176433
Score
-2.17039313
Score
0.0824594268
Score
-0.091365239
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000165667
RCV000819967
RCV002288749
ClinVar Variation:
186132
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Thr102Ile
CA000098
NM_000546.6:c.305C>T