Canonical Allele Identifier: PA2826567783
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Glu307Asp
CA397832446
NM_001276761.3:c.921G>T
CA397832451
NM_001276761.3:c.921G>C