Canonical Allele Identifier: PA2826565469
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 646725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Pro151Ser
CA397840839
NM_001276760.3:c.451C>T