Canonical Allele Identifier: PA916032836
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 185981
ClinVar RCV Id: RCV000165498 RCV000206887 RCV000590439 RCV000763700 RCV001798592 RCV003462176 RCV004552911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys1269Arg
CA193557
NM_001351834.2:c.3806A>G