ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579952057
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.1882436186
Score
-0.7952352678
Score
0.8201895075
Linked Data - NCBI & NCI
ClinVar RCV:
RCV002378947
RCV003621640
ClinVar Variation:
1766148
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ala307Pro
CA397836258
NM_000546.6:c.919G>C