Canonical Allele Identifier: PA2826562691
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Pro163Ser
CA336073
NM_001276697.3:c.487C>T