ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579936796
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.1490776366
Score
1.6123597047
Score
0.298770461
Score
-1.1383729258
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000492742
RCV000821569
RCV002289677
ClinVar Variation:
428902
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Asn131Ile
CA397842926
NM_000546.6:c.392A>T