Canonical Allele Identifier: PA916035100
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187317
ClinVar RCV Id: RCV000167036 RCV000526903 RCV003156228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile3040Thr
CA197338
NM_001351834.2:c.9119T>C