ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579934502
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.246976398
Score
0.9090102628
Score
-0.7954278902
Score
0.4803631493
Score
0.532310006
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000420461
RCV000425222
RCV000425855
RCV000430671
RCV000435260
RCV000435460
RCV000438306
RCV000443062
RCV000443210
RCV001027160
ClinVar Variation:
376598
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Phe270Val
CA16603020
NM_000546.6:c.808T>G