Canonical Allele Identifier: PA2826561657
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119726
ClinVar RCV Id: RCV003033239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Asn249Thr
CA397836634
NM_001276696.3:c.746A>C