Canonical Allele Identifier: PA916031554
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 480884
ClinVar RCV Id: RCV000572376 RCV001273625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile326Met
CA382531116
NM_001351834.2:c.978A>G