ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579951081
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.2633885022
Score
1.0494428071
Score
-1.4738360091
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000552096
ClinVar Variation:
458515
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ser362Cys
CA397831862
NM_000546.6:c.1084A>T