Canonical Allele Identifier: PA2826563990
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2703874
ClinVar RCV Id: RCV003510597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Pro32Leu
CA397840779
NM_001276699.3:c.95C>T