Canonical Allele Identifier: PA1139738992
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 834829
ClinVar RCV Id: RCV001035593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr1926Lys
CA382548300
NM_001351834.2:c.5777C>A