Canonical Allele Identifier: PA658673897
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His683Arg
CA382537439
NM_000051.4:c.2048A>G