Canonical Allele Identifier: PA916034916
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 822664
ClinVar RCV Id: RCV001018194 RCV002481825 RCV003605707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2897Asp
CA382523628
NM_001351834.2:c.8690G>A