ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936184
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.910508942
Score
1.0641755221
Score
-1.116955127
Score
0.7453815271
Score
-0.6374042275
Linked Data - NCBI & NCI
ClinVar Allele:
479353
ClinVar RCV:
RCV000570923
RCV001367015
RCV002272288
ClinVar Variation:
482230
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro152Ser
CA002580
NM_000546.6:c.454C>T