Canonical Allele Identifier: PA2825035968
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827432
ClinVar RCV Id: RCV001027138 RCV001315328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2691Gly
CA382562002
NM_000051.4:c.8071C>G