Canonical Allele Identifier: PA2826560662
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 634690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Phe74Cys
CA397844502
NM_001276696.3:c.221T>G
CA645589268
NM_001276696.3:c.221_222delinsGT