ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935411
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.5438955523
Score
1.4965891055
Score
0.243291467
Score
0.519841404
Score
1.5848923855
Score
0.255788991
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000417872
RCV000418906
RCV000423862
RCV000424176
RCV000426347
RCV000428105
RCV000428760
RCV000430958
RCV000433698
RCV000435531
RCV000436591
RCV000437249
RCV000438368
RCV000440868
RCV000441249
RCV000443239
ClinVar Variation:
376683
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Tyr205Ser
CA16603097
NM_000546.6:c.614A>C