Canonical Allele Identifier: PA645504338
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407608
ClinVar RCV Id: RCV000472748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2696Ile
CA16613495
NM_000051.4:c.8086G>A