ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936558
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.7752387464
Score
0.7860799978
Score
1.1049196929
Score
-0.278926931
Linked Data - NCBI & NCI
ClinVar Allele:
363546
ClinVar RCV:
RCV000419385
RCV000419630
RCV000423368
RCV000423812
RCV000424026
RCV000424710
RCV000425385
RCV000428977
RCV000429727
RCV000430321
RCV000432131
RCV000434737
RCV000436088
RCV000436286
RCV000436638
RCV000440402
RCV000440628
RCV000442028
RCV000442755
RCV000442833
RCV000492090
RCV000524926
RCV002289540
ClinVar Variation:
376667
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Thr125Arg
CA16044089
NM_000546.6:c.374C>G