ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579936751
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.510031885
Score
0.0126451101
Score
0.5286522209
Score
-1.538251645
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000576064
RCV000821053
RCV002289788
ClinVar Variation:
480741
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.His115Asn
CA397844462
NM_000546.6:c.343C>A