Canonical Allele Identifier: PA916035271
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127364
ClinVar RCV Id: RCV000115169 RCV000196996 RCV000515313 RCV000588846 RCV000855626 RCV001293035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Ser99Gly
CA286794
NM_001351836.2:c.295A>G