Canonical Allele Identifier: PA1139732821
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 856804
ClinVar RCV Id: RCV001062345 RCV003467817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser328Gly
CA382531146
NM_001351834.2:c.982A>G