ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579951116
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.6692203472
Score
-0.8847934664
Score
-0.541562095
Linked Data - NCBI & NCI
ClinVar Allele:
236441
ClinVar RCV:
RCV000213880
RCV000541338
RCV001537143
RCV002288853
ClinVar Variation:
230306
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly360Glu
CA10580905
NM_000546.6:c.1079G>A