Canonical Allele Identifier: PA191182
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 185157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro34Thr
CA000011
NM_001126112.3:c.100C>A