Canonical Allele Identifier: PA334657
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 188339
ClinVar RCV Id: RCV000168364 RCV000221360 RCV000236794 RCV003468831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr1871Ile
CA334655
NM_000051.4:c.5612C>T