ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935577
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.5148040999
Score
-2.899608316
Score
0.5499366258
Score
0.2560517067
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000633369
RCV001805766
RCV002289930
ClinVar Variation:
528262
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ala189Ser
CA397840875
NM_000546.6:c.565G>T