Canonical Allele Identifier: PA645435759
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 420136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro250Leu
CA16620620
NM_001126114.3:c.749C>T
CA645588533
NM_001126114.3:c.749_750delinsTT
CA645588536
NM_001126114.3:c.749_750delinsTG