Canonical Allele Identifier: PA913191734
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 627887
ClinVar RCV Id: RCV000771924 RCV001766600 RCV001856005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2235Val
CA6265997
NM_000051.4:c.6703A>G