Canonical Allele Identifier: PA916034539
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827323
ClinVar RCV Id: RCV001026937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2635Val
CA382561484
NM_001351834.2:c.7904C>T