Canonical Allele Identifier: PA658671215
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg3008Gly
CA382531129
NM_000051.4:c.9022C>G