Canonical Allele Identifier: PA169735
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142913
ClinVar RCV Id: RCV000132385 RCV000233534 RCV000236602 RCV001355326 RCV001197402 RCV002465534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg32Cys
CA169733
NM_000051.4:c.94C>T