Canonical Allele Identifier: PA2826561414
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg209Gln
CA000387
NM_001276696.3:c.626G>A
CA645588545
NM_001276696.3:c.626_627delinsAA