ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA336085
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.5275883806
Score
-0.3914152868
Score
-0.2599893851
Linked Data - NCBI & NCI
ClinVar Allele:
213387
ClinVar RCV:
RCV000195973
RCV000573146
RCV002288818
ClinVar Variation:
216475
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro322Ser
CA336073
NM_000546.6:c.964C>T