ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826564793
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000036530
RCV000131567
RCV000172826
RCV000590436
RCV000991144
RCV001355028
RCV002225273
RCV002496568
RCV003149630
ClinVar Variation:
43588
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263689.1:p.Pro8Ser
CA000053
NM_001276760.3:c.22C>T