Canonical Allele Identifier: PA2826561482
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Asp220His
CA397837641
NM_001276696.3:c.658G>C