ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA165052
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.071142577
Score
1.269661598
Score
-0.8442818557
Score
1.6094291489
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000129770
RCV000633376
RCV002288629
ClinVar Variation:
141302
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Phe113Val
CA000124
NM_000546.6:c.337T>G