ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA106934
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.8377893272
Score
0.6330198961
Score
-0.99503485
Score
1.3960858523
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000235571
RCV000492319
RCV000544036
ClinVar Variation:
245711
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Glu180Lys
CA10584590
NM_000546.6:c.538G>A