Canonical Allele Identifier: PA916035285
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453460
ClinVar RCV Id: RCV000528884 RCV003321643
ClinVar Variation Id: 1730081
ClinVar RCV Id: RCV003471332 RCV002454712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Ser111Arg
CA382521833
NM_001351836.2:c.331A>C
CA382521844
NM_001351836.2:c.333T>A
CA382521846
NM_001351836.2:c.333T>G