Canonical Allele Identifier: PA166952
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Arg26His
CA000227
NM_001126116.1:c.77G>A