ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579955030
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.5959084142
Score
-0.1097237329
Score
-0.8398046439
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000548671
RCV000563270
RCV000663228
RCV001704594
ClinVar Variation:
418693
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Glu11Lys
CA003910
NM_000546.6:c.31G>A