Canonical Allele Identifier: PA2826563083
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 423137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Cys23Trp
CA16620627
NM_001276698.3:c.69C>G