Canonical Allele Identifier: PA164995
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141284
ClinVar RCV Id: RCV000129735 RCV000230735 RCV001578023 RCV002478390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr3024Pro
CA164993
NM_000051.4:c.9070A>C