Canonical Allele Identifier: PA194189
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2179Met
CA194187
NM_000051.4:c.6537T>G