Canonical Allele Identifier: PA2741866278
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2568207
ClinVar RCV Id: RCV003297589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg667Lys
CA382537015
NM_001351834.2:c.2000G>A