Canonical Allele Identifier: PA2825035885
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 859210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2654Ser
CA382561712
NM_000051.4:c.7960A>T
CA382561715
NM_000051.4:c.7961C>G