Canonical Allele Identifier: PA2825035138
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 661649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2308Ser
CA382557094
NM_000051.4:c.6922G>T