ClinGen Allele Registry
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Canonical Allele Identifier:
PA192738
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.7786819626
Score
-1.714100856
Score
0.5653040368
Score
-0.4681744656
Score
0.629273342
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000165199
RCV000254809
RCV000456858
RCV001357202
RCV003474865
ClinVar Variation:
185722
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Cys277Tyr
CA000438
NM_000546.6:c.830G>A