ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935557
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.3206887861
Score
0.8159073119
Score
0.7305908662
Score
-1.141247876
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000222080
RCV001045782
RCV002288896
ClinVar Variation:
234061
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro190Arg
CA10580937
NM_000546.6:c.569C>G