Canonical Allele Identifier: PA2825033953
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 825668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys1782Glu
CA382543176
NM_000051.4:c.5344A>G