Canonical Allele Identifier: PA2826564397
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119726
ClinVar RCV Id: RCV003033239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Asn129Thr
CA397836634
NM_001276699.3:c.386A>C