Canonical Allele Identifier: PA891845327
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 571123
ClinVar RCV Id: RCV000692172 RCV000773334 RCV002060873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2223Val
CA228411958
NM_000051.4:c.6667A>G