Canonical Allele Identifier: PA2826561711
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469089
ClinVar RCV Id: RCV001993812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro262Ser
CA397836354
NM_001276696.3:c.784C>T