ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579951645
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.5674302002
Score
0.7993931353
Score
-0.4674490054
Linked Data - NCBI & NCI
ClinVar Allele:
479208
ClinVar RCV:
RCV000574074
RCV001043167
RCV002289807
ClinVar Variation:
481148
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Asp352Tyr
CA397832246
NM_000546.6:c.1054G>T