Canonical Allele Identifier: PA2826567369
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ile216Phe
CA16603041
NM_001276761.3:c.646A>T