ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579952188
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.1104274433
Score
0.1664218931
Score
-0.1298659352
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000566077
RCV001217424
RCV003476325
ClinVar Variation:
480952
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly325Glu
CA397835817
NM_000546.6:c.974G>A