Canonical Allele Identifier: PA2826562418
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 245777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Leu106Pro
CA10584586
NM_001276697.3:c.317T>C
CA645588450
NM_001276697.3:c.317_318delinsCT