Canonical Allele Identifier: PA2825034742
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1753441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2141Cys
CA382553499
NM_000051.4:c.6422C>G