Canonical Allele Identifier: PA2825032440
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1729985
ClinVar RCV Id: RCV002454701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys1101Glu
CA382517336
NM_000051.4:c.3301A>G