Canonical Allele Identifier: PA2499250754
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1001382
ClinVar RCV Id: RCV001297669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg189Ser
CA382527825
NM_001351834.2:c.567A>C
CA382527826
NM_001351834.2:c.567A>T