ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826560439
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000115715
RCV000122181
RCV000586104
RCV000662515
RCV001086750
RCV003492489
RCV003952551
ClinVar Variation:
127804
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263625.1:p.Pro19Arg
CA000061
NM_001276696.3:c.56C>G