Canonical Allele Identifier: PA2825035876
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2847879
ClinVar RCV Id: RCV003605235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro2648Leu
CA382561683
NM_000051.4:c.7943C>T