Canonical Allele Identifier: PA164002
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 140949
ClinVar RCV Id: RCV000129226 RCV001046782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Cys1838Arg
CA164000
NM_000051.4:c.5512T>C