Canonical Allele Identifier: PA2825617058
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2088334
ClinVar RCV Id: RCV003011589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Phe74_Gly78del
CA645589260
NM_001126118.1:c.219_233del