ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA107130
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.6376787995
Score
-0.104805853
Score
-1.771565144
Score
0.1432945114
Score
-0.3519243023
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013177
RCV001525191
ClinVar Variation:
12378
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Lys292Ile
CA000469
NM_000546.6:c.875A>T