Canonical Allele Identifier: PA916035184
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 422792
ClinVar RCV Id: RCV000479184 RCV000535900 RCV000775870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Ile40Val
CA16619094
NM_001351836.2:c.118A>G