Canonical Allele Identifier: PA2825031514
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1051352
ClinVar RCV Id: RCV001359376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly696Val
CA382537609
NM_000051.4:c.2087G>T