ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579953437
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.4479754282
Score
-0.0099157305
Score
0.0943789646
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000566433
RCV000811514
RCV002289782
ClinVar Variation:
480733
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro92Leu
CA397845138
NM_000546.6:c.275C>T