Canonical Allele Identifier: PA2826565496
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127817

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Leu155Phe
CA000278
NM_001276760.3:c.463C>T