Canonical Allele Identifier: PA2825031597
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2865130
ClinVar RCV Id: RCV003605497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr731Cys
CA382538920
NM_000051.4:c.2192A>G