Canonical Allele Identifier: PA2826566461
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ile11Thr
CA337284
NM_001276761.3:c.32T>C