ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579936950
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.677219506
Score
-0.971239926
Score
1.2004076819
Score
0.9213469071
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000434126
RCV004022449
ClinVar Variation:
389644
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Phe109Val
CA16608667
NM_000546.6:c.325T>G