Canonical Allele Identifier: PA2826563517
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Asp100Val
CA397837621
NM_001276698.3:c.299A>T
CA645588489
NM_001276698.3:c.299_300delinsTT