Canonical Allele Identifier: PA2826562024
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 100814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Arg37Leu
CA000284
NM_001276697.3:c.110G>T