Canonical Allele Identifier: PA2580203671
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1729803
ClinVar RCV Id: RCV002325086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1096Phe
CA382517254
NM_001351834.2:c.3288G>C
CA382517257
NM_001351834.2:c.3288G>T