Canonical Allele Identifier: PA916032641
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231546
ClinVar RCV Id: RCV000221075 RCV000524647 RCV000481285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys1114Arg
CA10579099
NM_001351834.2:c.3341A>G