Canonical Allele Identifier: PA165845
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141579
ClinVar RCV Id: RCV000130162 RCV000167957 RCV000236319 RCV000779778 RCV001798442 RCV003474759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2540Ile
CA165843
NM_000051.4:c.7618G>A