ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935409
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.6845031608
Score
1.5690996996
Score
-1.4880142171
Score
-0.105735609
Score
0.588418503
Score
-0.100804993
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000418952
RCV000419588
RCV000421235
RCV000421916
RCV000424047
RCV000426974
RCV000428672
RCV000429233
RCV000429897
RCV000431494
RCV000434394
RCV000436627
RCV000438926
RCV000439588
RCV000443853
RCV000443993
ClinVar Variation:
376682
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Tyr205Phe
CA16603096
NM_000546.6:c.614A>T