Canonical Allele Identifier: PA1139733338
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 965762
ClinVar RCV Id: RCV001240282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His448Tyr
CA382533746
NM_001351834.2:c.1342C>T