Canonical Allele Identifier: PA091792
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232389
ClinVar RCV Id: RCV000215525 RCV000800002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2702Arg
CA10579282
NM_000051.4:c.8105T>G