Allele Registry

Canonical Allele Identifier: PA2826566329

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000552096

ClinVar Variation:

458515

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263689.1:p.Ser323Cys	CA397831862 NM_001276760.3:c.967A>T