Canonical Allele Identifier: PA2825036486
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1382708
ClinVar RCV Id: RCV001890490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2896Arg
CA382523600
NM_000051.4:c.8687A>G