Canonical Allele Identifier: PA916033939
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489573
ClinVar RCV Id: RCV000580120 RCV003767268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2145Ala
CA382553566
NM_001351834.2:c.6434A>C