Canonical Allele Identifier: PA2825032833
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1171437
ClinVar RCV Id: RCV001524584 RCV001872039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1266Asn
CA382524657
NM_000051.4:c.3796G>A