Canonical Allele Identifier: PA2826561699
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1495821
ClinVar RCV Id: RCV001991580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Glu259Gln
CA397836431
NM_001276696.3:c.775G>C