Canonical Allele Identifier: PA916033251
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 184966
ClinVar RCV Id: RCV000164315 RCV000228294 RCV000994709 RCV003474856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg1618Gln
CA190612
NM_001351834.2:c.4853G>A