Canonical Allele Identifier: PA298082
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181898
ClinVar RCV Id: RCV000159661 RCV000168380 RCV000764950 RCV000569229 RCV001354380 RCV001526890 RCV003467223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2810Gln
CA298080
NM_000051.4:c.8428A>C