ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA107208
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.7132793047
Score
0.316487211
Score
0.545162285
Score
-1.4366645256
Score
0.064463068
Score
1.3612359279
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000214784
RCV000417969
RCV000419043
RCV000421915
RCV000423023
RCV000424153
RCV000428205
RCV000429345
RCV000430442
RCV000433311
RCV000434963
RCV000439555
RCV000440687
RCV000443824
RCV000785311
RCV001042706
RCV001374441
RCV001541668
ClinVar Variation:
232497
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro278Leu
CA10580915
NM_000546.6:c.833C>T