Canonical Allele Identifier: PA2826561514
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376605
ClinVar Variation Id: 458566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Gly227Arg
CA16603026
NM_001276696.3:c.679G>C
CA397837142
NM_001276696.3:c.679G>A
CA645588448
NM_001276696.3:c.678_679delinsAA