Canonical Allele Identifier: PA916031517
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 645269
ClinVar RCV Id: RCV000799317 RCV002370106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro292Arg
CA382529551
NM_001351834.2:c.875C>G