Canonical Allele Identifier: PA2573204367
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1463259
ClinVar RCV Id: RCV001960958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly670Val
CA382537072
NM_001351834.2:c.2009G>T