ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579951142
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.105107447
Score
-1.1745645508
Score
-0.7217800915
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000219841
RCV000249541
RCV000463320
RCV001557066
ClinVar Variation:
230534
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Glu358Val
CA000790
NM_000546.6:c.1073A>T