Canonical Allele Identifier: PA2826561689
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro256Ser
CA397836496
NM_001276696.3:c.766C>T