Canonical Allele Identifier: PA891844988
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 567035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His636Arg
CA382536307
NM_000051.4:c.1907A>G