ClinGen Allele Registry
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Canonical Allele Identifier:
PA164504
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0011133262
Score
-1.770746648
Score
-0.2940654075
Score
0.6812786526
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000129479
RCV000201000
RCV000228756
RCV002288625
ClinVar Variation:
141114
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly105Asp
CA000102
NM_000546.6:c.314G>A