Canonical Allele Identifier: PA2826563283
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 161397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Pro63Leu
CA000317
NM_001276698.3:c.188C>T
CA645588718
NM_001276698.3:c.187_188delinsTT