Canonical Allele Identifier: PA2826565109
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ser88Phe
CA000148
NM_001276760.3:c.263C>T
CA645589213
NM_001276760.3:c.263_264delinsTT