Canonical Allele Identifier: PA2825034022
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1495797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser1816Thr
CA382544194
NM_000051.4:c.5447G>C