Canonical Allele Identifier: PA2826561938
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.His20Arg
CA16603027
NM_001276697.3:c.59A>G