ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA130267
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.269969369
Score
0.2344365425
Score
-2.943488306
Score
1.1286230417
Score
0.0974708284
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000032610
RCV000692266
ClinVar Variation:
39420
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Arg181Leu
CA000262
NM_000546.6:c.542G>T