Canonical Allele Identifier: PA2825033977
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 825691
ClinVar RCV Id: RCV001024009 RCV001324515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1794Val
CA382543525
NM_000051.4:c.5380C>G