Canonical Allele Identifier: PA2826559038
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro33Ser
CA003069
NM_001276695.3:c.97C>T
CA2838032368
NM_001276695.3:c.97_98delinsAG