ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935192
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.2114838901
Score
1.7595941247
Score
0.370724095
Score
0.709056913
Score
0.324918933
Score
0.209933372
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000418001
RCV000419267
RCV000420351
RCV000424520
RCV000425133
RCV000425485
RCV000430145
RCV000431028
RCV000432729
RCV000435229
RCV000437599
RCV000438254
RCV000443153
ClinVar Variation:
376602
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly244Arg
CA16603024
NM_000546.6:c.730G>C