ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936333
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.5377103635
Score
-1.1679483494
Score
1.0977155351
Score
-0.722991182
Linked Data - NCBI & NCI
ClinVar Allele:
479330
ClinVar RCV:
RCV000562247
RCV002526919
ClinVar Variation:
486556
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val143Gly
CA397842510
NM_000546.6:c.428T>G