Canonical Allele Identifier: PA2825029992
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1001071
ClinVar RCV Id: RCV001297300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp18Asn
CA382519232
NM_000051.4:c.52G>A