ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2579951820
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.5825035243
Score
-0.9679277459
Score
-0.3844780157
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000584424
RCV002289878
RCV003767316
ClinVar Variation:
492627
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro318Leu
CA397835952
NM_000546.6:c.953C>T