Canonical Allele Identifier: PA2826566341
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 80708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.His326Tyr
CA000035
NM_001276760.3:c.976C>T