Canonical Allele Identifier: PA2580206540
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2040053
ClinVar RCV Id: RCV002886223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2613Ser
CA382561343
NM_001351834.2:c.7839A>C
CA382561344
NM_001351834.2:c.7839A>T