Canonical Allele Identifier: PA916033329
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524249
ClinVar RCV Id: RCV000627878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro1680Arg
CA382540338
NM_001351834.2:c.5039C>G