Canonical Allele Identifier: PA2825034132
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1009855
ClinVar RCV Id: RCV001307406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val1866Gly
CA382546216
NM_000051.4:c.5597T>G