Canonical Allele Identifier: PA2825598990
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro80Ser
CA16615999
NM_001126112.3:c.238C>T