Canonical Allele Identifier: PA658669665
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 479037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His1895Gln
CA228394526
NM_000051.4:c.5685C>A
CA382547757
NM_000051.4:c.5685C>G