Canonical Allele Identifier: PA658803186
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 528266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro77Ser
CA397845619
NM_001126114.3:c.229C>T