Canonical Allele Identifier: PA2825034749
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826400
ClinVar RCV Id: RCV001025261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu2145Gly
CA382553568
NM_000051.4:c.6434A>G