Canonical Allele Identifier: PA2826561917
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Cys17Ser
CA16602996
NM_001276697.3:c.49T>A
CA397841431
NM_001276697.3:c.50G>C
CA645588953
NM_001276697.3:c.48_49delinsTA
CA2695202323
NM_001276697.3:c.50_51delinsCT