ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826561157
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376686
ClinVar RCV Id:
RCV000421137
RCV000419128
RCV000423676
RCV000421350
RCV000426948
RCV000428535
RCV000428939
RCV000430021
RCV000434351
RCV000434446
RCV000438356
RCV000436740
RCV000439865
RCV000439629
RCV000444122
RCV000444873
RCV000462351
RCV000663307
RCV003441853
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263625.1:p.Tyr166Asp
CA16603100
NM_001276696.3:c.496T>G