Allele Registry

Canonical Allele Identifier: PA658679148

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 482211

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