ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826559732
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
135359
ClinVar RCV Id:
RCV000123099
RCV000122176
RCV000130072
RCV000144664
RCV000420459
RCV000420595
RCV000424188
RCV000430755
RCV000441015
RCV000420734
RCV000428223
RCV000430946
RCV000432016
RCV000436981
RCV000443346
RCV000444201
RCV000425846
RCV000427005
RCV000430601
RCV000438230
RCV000438582
RCV000419636
RCV000420908
RCV000422008
RCV000432438
RCV000437236
RCV000444077
RCV000626448
RCV001255672
RCV001798386
RCV003460862
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263624.1:p.Arg174Gln
CA000302
NM_001276695.3:c.521G>A