Canonical Allele Identifier: PA2580202557
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1779173
ClinVar RCV Id: RCV002401382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly335Val
CA382531383
NM_001351834.2:c.1004G>T