Canonical Allele Identifier: PA298298
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2032Lys
CA298296
NM_000051.4:c.6095G>A