Canonical Allele Identifier: PA091806
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231399
ClinVar RCV Id: RCV000220309 RCV000695412 RCV002264921 RCV003483578 RCV003469029
ClinVar Variation Id: 961847
ClinVar RCV Id: RCV001235608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2855Arg
CA6266378
NM_000051.4:c.8565T>A
CA6266379
NM_000051.4:c.8565T>G
CA382518596
NM_000051.4:c.8563A>C