Canonical Allele Identifier: PA2825030682
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 823522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg329Thr
CA382531217
NM_000051.4:c.986G>C