Canonical Allele Identifier: PA2827630125
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 418022
ClinVar RCV Id: RCV000480401 RCV000551041 RCV002418494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338764.1:p.Lys70Asn
CA16619095
NM_001351835.2:c.210A>T
CA382521298
NM_001351835.2:c.210A>C