Canonical Allele Identifier: PA2825607961
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482218
ClinVar Variation Id: 482235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Val203Leu
CA397840385
NM_001126114.3:c.607G>T
CA397840390
NM_001126114.3:c.607G>C