Canonical Allele Identifier: PA2826565275
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Thr116Ser
CA000210
NM_001276760.3:c.347C>G
CA397842094
NM_001276760.3:c.346A>T