Canonical Allele Identifier: PA2825034254
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 825958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly1925Arg
CA382548292
NM_000051.4:c.5773G>A
CA382548293
NM_000051.4:c.5773G>C