Canonical Allele Identifier: PA658679148
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ser33Tyr
CA397848079
NM_001126114.3:c.98C>A