Canonical Allele Identifier: PA916034170
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453655
ClinVar RCV Id: RCV000540394 RCV000570088 RCV002490927 RCV003330746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2339Lys
CA382558737
NM_001351834.2:c.7016G>A