Canonical Allele Identifier: PA2826565911
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Arg228Trp
CA000423
NM_001276760.3:c.682C>T