Canonical Allele Identifier: PA294067
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Thr312Ser
CA000505
NM_001126112.3:c.935C>G
CA397836079
NM_001126112.3:c.934A>T