Canonical Allele Identifier: PA2825600597
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 826488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro219Leu
CA397839907
NM_001126112.3:c.656C>T
CA645588728
NM_001126112.3:c.656_657delinsTT