Canonical Allele Identifier: PA165095
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141316
ClinVar RCV Id: RCV000129789 RCV000688954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn711Asp
CA165093
NM_000051.4:c.2131A>G