Canonical Allele Identifier: PA209572
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 210372
ClinVar RCV Id: RCV000195022 RCV003165429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr664Ala
CA209570
NM_000051.4:c.1990A>G