ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA195328
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.5047237301
Score
0.8377011921
Score
-0.9549270608
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000166233
RCV000559034
RCV002288759
ClinVar Variation:
186611
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Arg379Cys
CA000043
NM_000546.6:c.1135C>T