Canonical Allele Identifier: PA2580205900
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1756179
ClinVar RCV Id: RCV002378113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2308Gly
CA382557102
NM_001351834.2:c.6923C>G