Canonical Allele Identifier: PA916034110
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826672
ClinVar RCV Id: RCV001025744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2290Gly
CA382556768
NM_001351834.2:c.6869A>G