Canonical Allele Identifier: PA916034087
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181885
ClinVar RCV Id: RCV000219191 RCV000589270 RCV000456777 RCV002484994 RCV003226221 RCV003467220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2275Val
CA298040
NM_001351834.2:c.6823A>G