ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936121
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.2577940222
Score
1.532261479
Score
1.1263361969
Score
0.05796877
Linked Data - NCBI & NCI
ClinVar Allele:
245076
ClinVar RCV:
RCV000236862
RCV000548853
RCV000989719
RCV002288931
RCV002288932
ClinVar Variation:
246118
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Arg158Pro
CA10584592
NM_000546.6:c.473G>C