Canonical Allele Identifier: PA916032047
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181850
ClinVar RCV Id: RCV000159606 RCV000204474 RCV000174438 RCV002225458 RCV001356430 RCV004551366 RCV003477568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu699Gly
CA200987
NM_001351834.2:c.2096A>G