Canonical Allele Identifier: PA916034647
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181985
ClinVar RCV Id: RCV000159753 RCV000258960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val2716Phe
CA298328
NM_001351834.2:c.8146G>T