ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA106567
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.1879292716
Score
0.1057005605
Score
-0.0892301181
Score
-2.737837974
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ala138Ser
CA397842708
NM_000546.6:c.412G>T