Canonical Allele Identifier: PA2825035110
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1027190
ClinVar RCV Id: RCV001327751 RCV002368108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2298Ile
CA382556891
NM_000051.4:c.6892G>A