Canonical Allele Identifier: PA2825035854
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 926428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2636Ile
CA382561490
NM_000051.4:c.7907C>T