ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579934321
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.8048195843
Score
1.2351912139
Score
0.201408365
Score
0.083833867
Score
-1.5550663205
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000419239
RCV000424200
RCV000424885
RCV000425563
RCV000431443
RCV000432106
RCV000434236
RCV000436477
RCV000441480
RCV000443016
RCV000443884
RCV001229449
RCV003168618
ClinVar Variation:
376675
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val274Asp
CA16603089
NM_000546.6:c.821T>A