Canonical Allele Identifier: PA916033588
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 479037
ClinVar RCV Id: RCV000562812 RCV001066774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His1895Gln
CA228394526
NM_001351834.2:c.5685C>A
CA382547757
NM_001351834.2:c.5685C>G