Canonical Allele Identifier: PA658673276
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln65Arg
CA6264535
NM_000051.4:c.194A>G