Canonical Allele Identifier: PA2826561008
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1448445
ClinVar RCV Id: RCV001997129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys137del
CA397841425
NM_001276696.3:c.411C>A
CA645588951
NM_001276696.3:c.409_411del