Canonical Allele Identifier: PA2573204108
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1410688
ClinVar RCV Id: RCV001916528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg451Gly
CA382533778
NM_001351834.2:c.1351C>G