ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935298
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.232901341
Score
0.7377571149
Score
-2.075822468
Score
-1.636036879
Score
0.4659909149
Score
-0.4331929996
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000477098
RCV000564109
RCV003318578
ClinVar Variation:
406592
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro222Ser
CA16615720
NM_000546.6:c.664C>T