Canonical Allele Identifier: PA658801409
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524230
ClinVar RCV Id: RCV000627846 RCV000776375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile1167Val
CA382519746
NM_000051.4:c.3499A>G