Canonical Allele Identifier: PA2826561022
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.His139Pro
CA397841366
NM_001276696.3:c.416A>C