Canonical Allele Identifier: PA916034633
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407682
ClinVar RCV Id: RCV000457844 RCV002418373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2708His
CA16613497
NM_001351834.2:c.8122G>C