Canonical Allele Identifier: PA916033267
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481293
ClinVar RCV Id: RCV000570867 RCV001326586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val1629Met
CA382537189
NM_001351834.2:c.4885G>A