ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579937062
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.014440428
Score
-0.2042874186
Score
-2.100956934
Score
-1.687406584
Score
0.4665893987
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000492331
RCV001379190
RCV002289669
RCV004003474
ClinVar Variation:
428884
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly105Ser
CA397844735
NM_000546.6:c.313G>A