Canonical Allele Identifier: PA2825035711
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 646060
ClinVar RCV Id: RCV000800275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2568Lys
CA382561041
NM_000051.4:c.7703G>A