Canonical Allele Identifier: PA2825606788
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Leu111Pro
CA16603049
NM_001126114.3:c.332T>C