ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579951706
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.8933311763
Score
0.8273623749
Score
-0.3459090561
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000478385
RCV000555965
RCV000573045
RCV002289633
ClinVar Variation:
420950
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Asp324His
CA16620612
NM_000546.6:c.970G>C