Canonical Allele Identifier: PA916033081
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 633052
ClinVar RCV Id: RCV000780884 RCV003480812 RCV003500600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1476Val
CA382532274
NM_001351834.2:c.4426A>G