Canonical Allele Identifier: PA916031672
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181918
ClinVar RCV Id: RCV000159683 RCV000628061 RCV003162670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln404Glu
CA298138
NM_001351834.2:c.1210C>G