ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA287814
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.369558859
Score
-1.177448585
Score
1.1041548767
Score
2.4428389288
Linked Data - NCBI & NCI
ClinVar Allele:
133279
ClinVar RCV:
RCV000115734
RCV001344441
RCV002381420
ClinVar Variation:
127822
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Met246Arg
CA000376
NM_000546.6:c.737T>G