Canonical Allele Identifier: PA916034123
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 421478
ClinVar RCV Id: RCV000485190 RCV000560466 RCV001025791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2303Met
CA16619222
NM_001351834.2:c.6908A>T