ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579952053
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.8792767541
Score
0.6312797852
Score
-0.1962001778
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000824567
RCV002372364
ClinVar Variation:
666137
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ala307Val
CA397836165
NM_000546.6:c.920C>T