Canonical Allele Identifier: PA916032039
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524244
ClinVar RCV Id: RCV000627872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu690Pro
CA382537515
NM_001351834.2:c.2069T>C