ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA300329
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.5505116828
Score
0.381332355
Score
0.3950565359
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000161064
RCV001850278
RCV002288701
RCV002288702
ClinVar Variation:
182962
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val97Leu
CA000092
NM_000546.6:c.289G>C