Canonical Allele Identifier: PA916031514
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453744
ClinVar RCV Id: RCV000556761 RCV001018241 RCV001174585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His291Arg
CA382529539
NM_001351834.2:c.872A>G