ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579936816
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.2614098307
Score
1.4047194144
Score
0.120130531
Score
0.8740569777
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000492142
RCV002475970
ClinVar Variation:
428873
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu130Pro
CA397842949
NM_000546.6:c.389T>C