Canonical Allele Identifier: PA1139738734
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 968054
ClinVar RCV Id: RCV001243102 RCV001760273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly1817Glu
CA382544227
NM_001351834.2:c.5450G>A