Canonical Allele Identifier: PA2825031452
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1784106
ClinVar RCV Id: RCV002417043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg667Gly
CA382537011
NM_000051.4:c.1999A>G