Canonical Allele Identifier: PA2825034543
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1500436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2053Arg
CA382550624
NM_000051.4:c.6158C>G