ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA167419
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.6935609566
Score
0.5651793009
Score
-0.2048798703
Linked Data - NCBI & NCI
ClinVar Allele:
151819
ClinVar RCV:
RCV000130938
RCV001229943
RCV002288643
ClinVar Variation:
142105
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Glu358Lys
CA000027
NM_000546.6:c.1072G>A