Canonical Allele Identifier: PA287003
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127451
ClinVar RCV Id: RCV000115257 RCV000475783 RCV002415591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2633Val
CA287001
NM_000051.4:c.7897T>G