Canonical Allele Identifier: PA658673580
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 480884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile326Met
CA382531116
NM_000051.4:c.978A>G