ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579952697
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.2515085412
Score
1.6859554418
Score
0.196210821
Score
0.8672210793
Score
0.292829412
Linked Data - NCBI & NCI
ClinVar Allele:
467516
ClinVar RCV:
RCV000540536
RCV003159760
RCV004023790
ClinVar Variation:
458562
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu257Pro
CA397837703
NM_000546.6:c.770T>C