Canonical Allele Identifier: PA916035172
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181945
ClinVar RCV Id: RCV000562263 RCV000459267 RCV001721017 RCV002288671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Arg32His
CA298213
NM_001351836.2:c.95G>A