Canonical Allele Identifier: PA167001
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141976
ClinVar RCV Id: RCV000130731 RCV000205355 RCV000481018 RCV003461998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro1680Leu
CA166999
NM_000051.4:c.5039C>T