Canonical Allele Identifier: PA2825608789
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Glu258Asp
CA397837660
NM_001126114.3:c.774A>T
CA397837662
NM_001126114.3:c.774A>C