Canonical Allele Identifier: PA916033672
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 479081
ClinVar RCV Id: RCV000561373 RCV000685483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1963Gly
CA382548540
NM_001351834.2:c.5888A>G