Canonical Allele Identifier: PA2826562388
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Glu99Asp
CA397837660
NM_001276697.3:c.297A>T
CA397837662
NM_001276697.3:c.297A>C