ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935249
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.113593553
Score
-3.228843066
Score
-2.298961198
Score
0.1117072847
Score
0.0501615319
Score
0.2397086317
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000567074
RCV000759379
RCV002289814
RCV002530256
ClinVar Variation:
482214
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ile232Leu
CA397839370
NM_000546.6:c.694A>C