Canonical Allele Identifier: PA916031563
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg329Lys
CA6264714
NM_001351834.2:c.986G>A