Canonical Allele Identifier: PA916031582
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 133643
ClinVar RCV Id: RCV000120170 RCV000167222 RCV000234064 RCV000657017 RCV002288608 RCV003492519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val341Ile
CA157207
NM_001351834.2:c.1021G>A