Canonical Allele Identifier: PA2825602708
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Pro27Thr
CA16615735
NM_001126113.3:c.79C>A