Canonical Allele Identifier: PA916031559
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232166
ClinVar RCV Id: RCV000213925 RCV000627952 RCV003469052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser328del
CA10578988
NM_001351834.2:c.984_986del