Canonical Allele Identifier: PA2825031398
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3232231
ClinVar RCV Id: RCV004520914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu641Val
CA382536462
NM_000051.4:c.1922A>T