ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826566016
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
182938
ClinVar RCV Id:
RCV000161038
RCV000213059
RCV000633381
RCV001527101
RCV003150958
RCV003467273
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263689.1:p.Arg243Leu
CA000456
NM_001276760.3:c.728G>T