ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579952433
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.2259872073
Score
0.241762828
Score
0.2824738047
Score
-1.3871893439
Score
-1.598133365
Linked Data - NCBI & NCI
ClinVar Allele:
410260
ClinVar RCV:
RCV000480494
RCV000819627
RCV002248705
RCV002431408
ClinVar Variation:
421804
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Cys277Arg
CA16620617
NM_000546.6:c.829T>C