ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826562578
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
127825
ClinVar RCV Id:
RCV000115740
RCV000148914
RCV000213061
RCV001357075
RCV001798340
RCV000620742
RCV003935102
RCV000760102
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263626.1:p.Arg131His
CA000468
NM_001276697.3:c.392G>A