Canonical Allele Identifier: PA2825034007
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1747451
ClinVar RCV Id: RCV002349503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr1808Ile
CA382543953
NM_000051.4:c.5423C>T