Canonical Allele Identifier: PA355427
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 219883
ClinVar RCV Id: RCV000204577 RCV002354574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2018Ser
CA348802
NM_000051.4:c.6053T>C