Canonical Allele Identifier: PA194799
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186433
ClinVar RCV Id: RCV000166025 RCV000232405 RCV001571325 RCV003462197 RCV003493474 RCV003491904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile1806Thr
CA194797
NM_000051.4:c.5417T>C