Canonical Allele Identifier: PA2825036494
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 822665
ClinVar RCV Id: RCV001018195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2899Val
CA382523659
NM_000051.4:c.8695A>G