Canonical Allele Identifier: PA2826560701
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182926
ClinVar Variation Id: 1021578
ClinVar RCV Id: RCV001321369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys85Ser
CA000138
NM_001276696.3:c.253T>A
CA397844266
NM_001276696.3:c.254G>C