Canonical Allele Identifier: PA2826562755
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Phe179Leu
CA000848
NM_001276697.3:c.537C>G
CA397832711
NM_001276697.3:c.537C>A
CA397832735
NM_001276697.3:c.535T>C