Canonical Allele Identifier: PA891845026
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 566646
ClinVar RCV Id: RCV000686514 RCV000777893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala869Glu
CA6265066
NM_000051.4:c.2606C>A