Canonical Allele Identifier: PA286999
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127449
ClinVar RCV Id: RCV000115255 RCV000197623 RCV000588147 RCV001257470 RCV002228249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2593Arg
CA286997
NM_000051.4:c.7778A>G