Canonical Allele Identifier: PA2499251098
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 999524
ClinVar RCV Id: RCV001295534 RCV001773600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser179Leu
CA382527625
NM_001351834.2:c.536C>T