Canonical Allele Identifier: PA2580206781
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1714080
ClinVar RCV Id: RCV002297063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2729Arg
CA382562529
NM_001351834.2:c.8186A>G