Canonical Allele Identifier: PA2825615637
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Gly113Val
CA001743
NM_001126117.1:c.338G>T
CA645588573
NM_001126117.1:c.338_339delinsTT