Canonical Allele Identifier: PA916032224
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 821379
ClinVar RCV Id: RCV001015732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu834Lys
CA382543305
NM_001351834.2:c.2500G>A