ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA191181
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.6748876497
Score
-0.6014895163
Score
-0.0867920653
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000164526
RCV000471959
RCV001582646
RCV002288737
ClinVar Variation:
185157
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro34Thr
CA000011
NM_000546.6:c.100C>A