Canonical Allele Identifier: PA2826559922
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428865
ClinVar RCV Id: RCV000492700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.[Gly205_Asn208del;Arg210del]
CA645369701
NM_001276695.3:c.613_627del