Canonical Allele Identifier: PA2826566913
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Cys137Ser
CA16602996
NM_001276761.3:c.409T>A
CA397841431
NM_001276761.3:c.410G>C
CA645588953
NM_001276761.3:c.408_409delinsTA
CA2695202323
NM_001276761.3:c.410_411delinsCT