Canonical Allele Identifier: PA2825035089
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1714289
ClinVar RCV Id: RCV002297245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Trp2291Gly
CA382556774
NM_000051.4:c.6871T>G