ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA162499
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.599485408
Score
0.2556216761
Score
-2.68290729
Score
-2.301151433
Score
-0.5088338643
Score
0.5259264932
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000122175
RCV000459232
RCV000567735
RCV001030735
RCV001358628
ClinVar Variation:
135358
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Arg202His
CA000289
NM_000546.6:c.605G>A