Canonical Allele Identifier: PA2826559279
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Leu91Phe
CA339065
NM_001276695.3:c.271C>T