Canonical Allele Identifier: PA916006629
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 419837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Thr79Ile
CA16620635
NM_001276761.3:c.236C>T