Canonical Allele Identifier: PA916032199
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186370
ClinVar RCV Id: RCV000165954 RCV000627939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala823Ser
CA194637
NM_001351834.2:c.2467G>T