ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935723
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.8496553422
Score
0.249550718
Score
-1.4419052271
Score
1.2277115948
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000419057
RCV000423937
RCV000424516
RCV000425646
RCV000426810
RCV000433343
RCV000433582
RCV000436323
RCV000441162
RCV000441887
RCV000442808
RCV000633391
ClinVar Variation:
376635
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu194Pro
CA16603053
NM_000546.6:c.581T>C