Canonical Allele Identifier: PA2825617767
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Pro138Leu
CA16615728
NM_001126118.1:c.413C>T
CA645588942
NM_001126118.1:c.413_414delinsTT