ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935265
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.058840373
Score
-2.898774798
Score
-2.259657792
Score
0.5193481882
Score
-0.3233745913
Score
-1.861830257
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000464185
RCV000562254
RCV002289590
ClinVar Variation:
406567
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Met243Val
CA16615711
NM_000546.6:c.727A>G