Canonical Allele Identifier: PA2826567159
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro183Ser
CA16615720
NM_001276761.3:c.547C>T