ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935428
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.225729842
Score
-2.072223343
Score
1.1116879901
Score
-2.635677848
Score
0.0853132692
Score
-1.0364000767
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000218191
RCV003509516
ClinVar Variation:
231661
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Arg202Gly
CA10580933
NM_000546.6:c.604C>G