Canonical Allele Identifier: PA2826565499
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ile156Thr
CA002232
NM_001276760.3:c.467T>C