Canonical Allele Identifier: PA658670571
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481332
ClinVar RCV Id: RCV000563057 RCV001058181 RCV001558673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2629Met
CA6266206
NM_000051.4:c.7887A>G