ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936396
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.8798452085
Score
0.0697984411
Score
-2.092748828
Score
0.0939096557
Linked Data - NCBI & NCI
ClinVar Allele:
468396
ClinVar RCV:
RCV000534841
RCV001563388
RCV002289732
RCV002289733
ClinVar Variation:
458544
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Thr155Ala
CA002539
NM_000546.6:c.463A>G