Canonical Allele Identifier: PA2826567739
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg296Cys
CA000009
NM_001276761.3:c.886C>T