ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579953521
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.25289038
Score
-1.3534162102
Score
0.6109524395
Linked Data - NCBI & NCI
ClinVar Allele:
479350
ClinVar RCV:
RCV000565147
RCV001322778
RCV002289783
ClinVar Variation:
480734
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ala88Val
CA397845305
NM_000546.6:c.263C>T