Canonical Allele Identifier: PA916035221
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481162
ClinVar RCV Id: RCV000567749 RCV000707181 RCV003235290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Gln65Arg
CA6264535
NM_001351836.2:c.194A>G