ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935352
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.5504753527
Score
-3.171483246
Score
-2.25897459
Score
0.0466431289
Score
-0.2680304495
Score
-1.953757818
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000542075
RCV000572327
RCV001591203
RCV002289739
ClinVar Variation:
458556
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly226Val
CA287488077
NM_000546.6:c.677G>T