ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579955278
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.5843224814
Score
0.3389214212
Score
-0.1514453272
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000633363
RCV000772527
RCV002289926
ClinVar Variation:
528258
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro12Leu
CA397849144
NM_000546.6:c.35C>T