Canonical Allele Identifier: PA167122
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Ser215Thr
CA000307
NM_001126113.3:c.644G>C