Canonical Allele Identifier: PA916033702
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 234219
ClinVar RCV Id: RCV000222930 RCV000235262 RCV000234260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1986Val
CA10579202
NM_001351834.2:c.5956A>G