Canonical Allele Identifier: PA916032217
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 572939
ClinVar RCV Id: RCV000694461 RCV001015701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg832Gly
CA382543254
NM_001351834.2:c.2494C>G