Canonical Allele Identifier: PA2826564427
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Pro136Ser
CA397836496
NM_001276699.3:c.406C>T