ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579936456
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.7271582298
Score
-0.3216162326
Score
-0.2819901866
Score
-2.780926649
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001302774
ClinVar Variation:
1005829
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu137Val
CA397842729
NM_000546.6:c.409C>G