Canonical Allele Identifier: PA2580204744
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1718388
ClinVar RCV Id: RCV002304889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys1838Ser
CA382545743
NM_001351834.2:c.5512T>A
CA382545754
NM_001351834.2:c.5513G>C