Canonical Allele Identifier: PA165989
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141634
ClinVar RCV Id: RCV000130230 RCV000196159 RCV000254719 RCV002281955 RCV003162582 RCV003467134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg3008His
CA165987
NM_000051.4:c.9023G>A