Canonical Allele Identifier: PA658679578
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Val93Ile
CA397839539
NM_001126117.1:c.277G>A