Canonical Allele Identifier: PA1139732433
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 631197
ClinVar RCV Id: RCV000777359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala235del
CA913188427
NM_001351834.2:c.702_704del