Canonical Allele Identifier: PA2826563708
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718571
ClinVar RCV Id: RCV002299896
ClinVar Variation Id: 2679235
ClinVar RCV Id: RCV003464702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Lys133Asn
CA397836532
NM_001276698.3:c.399A>T
CA397836533
NM_001276698.3:c.399A>C