Canonical Allele Identifier: PA2825034559
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2061Pro
CA382550735
NM_000051.4:c.6182A>C