Canonical Allele Identifier: PA2826565439
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 423137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Cys143Trp
CA16620627
NM_001276760.3:c.429C>G