Canonical Allele Identifier: PA916031989
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 135739
ClinVar RCV Id: RCV000122828 RCV000165083 RCV000254742 RCV001354480 RCV003320097 RCV003467083 RCV003492531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln654Lys
CA192475
NM_001351834.2:c.1960C>A