Canonical Allele Identifier: PA916034102
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524233
ClinVar RCV Id: RCV000627849 RCV001288456 RCV001025737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2287Arg
CA382556715
NM_001351834.2:c.6859G>A
CA382556716
NM_001351834.2:c.6859G>C