Canonical Allele Identifier: PA916031727
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482610
ClinVar RCV Id: RCV000566516 RCV001343094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His448Arg
CA382533748
NM_001351834.2:c.1343A>G