Canonical Allele Identifier: PA2573071152
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1306194
ClinVar RCV Id: RCV001767147 RCV003500683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser933Tyr
CA382545652
NM_001351834.2:c.2798C>A