Canonical Allele Identifier: PA2826563602
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Cys116Trp
CA397836936
NM_001276698.3:c.348T>G