ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936941
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0216205203
Score
-0.475824992
Score
0.2432945
Score
0.6226524788
Score
0.1586580045
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000473145
RCV000492590
RCV000785348
RCV002289602
RCV004000748
ClinVar Variation:
406597
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Arg110Leu
CA002845
NM_000546.6:c.329G>T