Canonical Allele Identifier: PA2825035997
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1361515
ClinVar RCV Id: RCV001899710 RCV002422912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2700Glu
CA382562095
NM_000051.4:c.8098A>G