Canonical Allele Identifier: PA2826561420
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12352
ClinVar Variation Id: 406598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg210Ser
CA000392
NM_001276696.3:c.630G>T
CA16615944
NM_001276696.3:c.630G>C