Canonical Allele Identifier: PA916032906
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 419344
ClinVar RCV Id: RCV000483145 RCV001021605 RCV001274266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1332Ser
CA16619172
NM_001351834.2:c.3995T>G