Canonical Allele Identifier: PA2825035151
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2839642
ClinVar RCV Id: RCV003605109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2314Arg
CA382557243
NM_000051.4:c.6941A>G