ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935369
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.587840347
Score
-1.0786453277
Score
-0.760732494
Score
-0.246175532
Score
1.5691490839
Score
0.9206436919
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000796697
RCV002256509
RCV002290436
ClinVar Variation:
643078
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.His214Pro
CA397840046
NM_000546.6:c.641A>C