Canonical Allele Identifier: PA2826561886
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2446885
ClinVar RCV Id: RCV003159585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Glu12Asp
CA397841579
NM_001276697.3:c.36G>T
CA397841581
NM_001276697.3:c.36G>C