Canonical Allele Identifier: PA2826564486
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Asn152Ser
CA16615690
NM_001276699.3:c.455A>G