Canonical Allele Identifier: PA2826559202
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 823709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Phe74Ser
CA397844504
NM_001276695.3:c.221T>C