Canonical Allele Identifier: PA2826566409
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Thr348Arg
CA287485465
NM_001276760.3:c.1043C>G