Canonical Allele Identifier: PA2826565478
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2703874
ClinVar RCV Id: RCV003510597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Pro152Leu
CA397840779
NM_001276760.3:c.455C>T