Canonical Allele Identifier: PA2826562316
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Asn88Ser
CA16615997
NM_001276697.3:c.263A>G