Canonical Allele Identifier: PA2580206515
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1760706
ClinVar RCV Id: RCV002409925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2602Gly
CA382561271
NM_001351834.2:c.7805C>G