ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935405
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.649511804
Score
-3.47653588
Score
-2.379230218
Score
0.5263694858
Score
-0.4271359723
Score
-0.2529976397
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000507226
RCV000566251
RCV001049540
ClinVar Variation:
439319
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu206Ser
CA397840264
NM_000546.6:c.617T>C