Canonical Allele Identifier: PA2825035863
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1444446
ClinVar RCV Id: RCV001992357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2641Glu
CA382561517
NM_000051.4:c.7921C>G