Canonical Allele Identifier: PA2826559734
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Arg174Leu
CA16603067
NM_001276695.3:c.521G>T