Canonical Allele Identifier: PA2827629221
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3222669
ClinVar RCV Id: RCV004516053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2311del
CA2825001938
NM_001351834.2:c.6931_6933del