Canonical Allele Identifier: PA286731
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127338
ClinVar RCV Id: RCV000115142 RCV000197378 RCV000211962 RCV000779759 RCV001762217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys482Gln
CA286729
NM_000051.4:c.1444A>C