Canonical Allele Identifier: PA916033921
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 631338
ClinVar RCV Id: RCV000777525 RCV003318636 RCV003607356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2128Ser
CA382553298
NM_001351834.2:c.6383T>C