Canonical Allele Identifier: PA916032260
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp851Gly
CA6265058
NM_001351834.2:c.2552A>G