Canonical Allele Identifier: PA916032696
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453470
ClinVar RCV Id: RCV000558586 RCV002341233 RCV003470667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1163Tyr
CA6265299
NM_001351834.2:c.3488C>A