Canonical Allele Identifier: PA2825035132
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 843322
ClinVar RCV Id: RCV001045919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2307His
CA382557083
NM_000051.4:c.6920T>A