Canonical Allele Identifier: PA2825608216
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro222Ser
CA16615720
NM_001126114.3:c.664C>T