Canonical Allele Identifier: PA2826566127
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1471105
ClinVar RCV Id: RCV001995379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Pro270Leu
CA397836130
NM_001276760.3:c.809C>T