Canonical Allele Identifier: PA2825034701
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2125874
ClinVar RCV Id: RCV003043838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2122Ile
CA382553217
NM_000051.4:c.6365C>T