Canonical Allele Identifier: PA645503419
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 234231
ClinVar RCV Id: RCV000219697 RCV001371515 RCV001311788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr1926Ile
CA10579197
NM_000051.4:c.5777C>T