Canonical Allele Identifier: PA2826564398
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439164
ClinVar RCV Id: RCV001958047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Leu130Ile
CA397836621
NM_001276699.3:c.388C>A