Canonical Allele Identifier: PA166350
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg135Trp
CA000423
NM_001126115.1:c.403C>T