Canonical Allele Identifier: PA1139735661
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 922591
ClinVar RCV Id: RCV001182720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala920Glu
CA6265108
NM_001351834.2:c.2759C>A