Canonical Allele Identifier: PA2827635456
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3222400
ClinVar RCV Id: RCV004513814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2185Val
CA382554352
NM_001351834.2:c.6553A>G