Canonical Allele Identifier: PA916032008
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 419317
ClinVar RCV Id: RCV000481061 RCV000627944 RCV000772636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile665Thr
CA16619131
NM_001351834.2:c.1994T>C