Canonical Allele Identifier: PA2825034009
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1692780
ClinVar RCV Id: RCV002258634 RCV003605779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1809Val
CA382543966
NM_000051.4:c.5425C>G