Canonical Allele Identifier: PA2826560439
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127804
ClinVar RCV Id: RCV000115715 RCV000122181 RCV000662515 RCV000586104 RCV001086750 RCV003492489 RCV003952551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro19Arg
CA000061
NM_001276696.3:c.56C>G