Allele Registry

Canonical Allele Identifier: PA2826564496

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 406587

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263628.1:p.Ser155Phe	CA001234 NM_001276699.3:c.464C>T