ClinGen Allele Registry
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Canonical Allele Identifier:
PA287768
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.529342953
Score
-1.806826964
Score
0.7022030771
Score
-0.0696591333
Score
-1.0594007665
Score
-2.074972357
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000115729
RCV000473040
RCV000563913
RCV001257499
ClinVar Variation:
127818
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Arg202Cys
CA000288
NM_000546.6:c.604C>T