ClinGen Allele Registry
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Canonical Allele Identifier:
PA162558
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.790946896
Score
0.5132179059
Score
0.2012898883
Score
-0.2454386934
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000115719
RCV000122182
RCV000228299
RCV000409407
RCV000589869
RCV001358219
ClinVar Variation:
127808
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Arg110His
CA000123
NM_000546.6:c.329G>A