Canonical Allele Identifier: PA916033067
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181996
ClinVar RCV Id: RCV000159765 RCV000206187 RCV000220574 RCV003467242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1465Pro
CA298357
NM_001351834.2:c.4394T>C