Canonical Allele Identifier: PA2826562616
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765377
ClinVar RCV Id: RCV002376305

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Pro141Leu
CA287486577
NM_001276697.3:c.422C>T