Canonical Allele Identifier: PA916031603
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127329
ClinVar RCV Id: RCV000115133 RCV000196425 RCV000211956 RCV000587788 RCV001355543 RCV002221486 RCV001798306 RCV004549537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn358Ser
CA286708
NM_001351834.2:c.1073A>G