Canonical Allele Identifier: PA165669
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141518
ClinVar RCV Id: RCV000130083 RCV000458854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp841Gly
CA165667
NM_000051.4:c.2522A>G