ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579934363
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.41610079
Score
1.0895786775
Score
0.590676363
Score
-1.3690104768
Score
1.6994249364
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000492273
RCV000691629
RCV003326137
ClinVar Variation:
428867
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Arg267Pro
CA397837115
NM_000546.6:c.800G>C