ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA166910
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.1026070155
Score
0.5156164825
Score
-0.104944799
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000130694
RCV001303642
RCV002288640
ClinVar Variation:
141956
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ala83Glu
CA000082
NM_000546.6:c.248C>A