ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA165857
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.4692191567
Score
-0.0221490871
Score
-1.0587168954
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000130166
RCV001313040
RCV003474760
ClinVar Variation:
141583
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly374Ser
CA000040
NM_000546.6:c.1120G>A