Canonical Allele Identifier: PA916032817
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 650877
ClinVar RCV Id: RCV000806117 RCV003362958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1256Met
CA6265351
NM_001351834.2:c.3768T>G