Canonical Allele Identifier: PA658674152
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 479053
ClinVar RCV Id: RCV000628118 RCV000562509 RCV000679106 RCV003321672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu906Met
CA382545292
NM_000051.4:c.2716T>A