Canonical Allele Identifier: PA916034548
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231842
ClinVar RCV Id: RCV000222696 RCV002221518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2640Ser
CA10579274
NM_001351834.2:c.7919C>G
CA382561513
NM_001351834.2:c.7918A>T