Canonical Allele Identifier: PA1139729753
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 921131
ClinVar RCV Id: RCV001180350 RCV001875983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2623Ile
CA382561404
NM_001351834.2:c.7867C>A