Canonical Allele Identifier: PA916034516
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187688
ClinVar RCV Id: RCV000167438 RCV000469981 RCV000480349 RCV003474890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2622Gly
CA198312
NM_001351834.2:c.7865C>G