Canonical Allele Identifier: PA2825034763
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 845717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2150Thr
CA382553659
NM_000051.4:c.6448G>A