Canonical Allele Identifier: PA2573204387
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1489968
ClinVar RCV Id: RCV001983520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val682Phe
CA382537426
NM_001351834.2:c.2044G>T