Canonical Allele Identifier: PA916034490
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 557639
ClinVar RCV Id: RCV000673806 RCV002406516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2597Tyr
CA382561238
NM_001351834.2:c.7789G>T