ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579951716
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.9156557182
Score
-0.7408983207
Score
-1.1710629526
Linked Data - NCBI & NCI
ClinVar RCV:
RCV003464701
ClinVar Variation:
2679234
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu323Val
CA397835860
NM_000546.6:c.967C>G