Canonical Allele Identifier: PA2826562597
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Pro136Ser
CA397836496
NM_001276697.3:c.406C>T