Canonical Allele Identifier: PA2580202520
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1768233
ClinVar RCV Id: RCV002387217 RCV003094875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly327Arg
CA382531118
NM_001351834.2:c.979G>A
CA382531125
NM_001351834.2:c.979G>C