Canonical Allele Identifier: PA2826559660
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 100814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Arg157Leu
CA000284
NM_001276695.3:c.470G>T