Canonical Allele Identifier: PA2580204733
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2158108
ClinVar RCV Id: RCV003093454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val1833Gly
CA382545640
NM_001351834.2:c.5498T>G