Canonical Allele Identifier: PA2825036046
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1495088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2717Thr
CA382562263
NM_000051.4:c.8150A>C