Allele Registry

Canonical Allele Identifier: PA2826567662

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 406587

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Ser275Phe	CA001234 NM_001276761.3:c.824C>T