Canonical Allele Identifier: PA2826567345
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Leu213Pro
CA000398
NM_001276761.3:c.638T>C