Canonical Allele Identifier: PA916033511
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233538
ClinVar RCV Id: RCV000215343 RCV000533648 RCV000486930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe1837Val
CA10579183
NM_001351834.2:c.5509T>G