Canonical Allele Identifier: PA165680
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg1095Lys
CA165678
NM_000051.4:c.3284G>A