Canonical Allele Identifier: PA2580203026
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1777837
ClinVar RCV Id: RCV002414519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu560Lys
CA382535143
NM_001351834.2:c.1678G>A