ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2579951465
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.0885275392
Score
0.2219845105
Score
-0.8407389596
Linked Data - NCBI & NCI
ClinVar Allele:
420637
ClinVar RCV:
RCV000492343
RCV002289665
ClinVar Variation:
428876
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly334Trp
CA397832878
NM_000546.6:c.1000G>T