Canonical Allele Identifier: PA2826561991
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 646725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Pro31Ser
CA397840839
NM_001276697.3:c.91C>T