ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA106558
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.2951372175
Score
0.9524567693
Score
-1.4719831691
Score
0.386777613
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013175
RCV000461233
RCV002326677
ClinVar Variation:
12376
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ala138Pro
CA000166
NM_000546.6:c.412G>C