Canonical Allele Identifier: PA2826561165
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 439319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Leu167Ser
CA397840264
NM_001276696.3:c.500T>C