Canonical Allele Identifier: PA2826564255
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Arg108Trp
CA000423
NM_001276699.3:c.322C>T