Canonical Allele Identifier: PA658803168
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 528258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro12Leu
CA397849144
NM_001126114.3:c.35C>T