ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579953771
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.1745649338
Score
-0.4061167483
Score
0.3765622137
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000633383
RCV001015102
RCV002289932
ClinVar Variation:
528266
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro77Ser
CA397845619
NM_000546.6:c.229C>T