Canonical Allele Identifier: PA2825032029
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 845319
ClinVar RCV Id: RCV001048361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile923Met
CA382545511
NM_000051.4:c.2769T>G