ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA167496
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.1422641483
Score
0.660262954
Score
1.8910353961
Score
0.209971121
Score
-1.1994717928
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000130981
RCV001233712
ClinVar Variation:
142134
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu257Arg
CA000404
NM_000546.6:c.770T>G