Canonical Allele Identifier: PA916033845
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 234090
ClinVar RCV Id: RCV000217659 RCV000456769 RCV002288898 RCV002494598 RCV003441803 RCV003488480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2076Val
CA6265897
NM_001351834.2:c.6226A>G