Canonical Allele Identifier: PA2826566651
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 3148392
ClinVar RCV Id: RCV004440297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Phe70_Arg71del
CA645589280
NM_001276761.3:c.208_213del