Canonical Allele Identifier: PA2580202801
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1770633
ClinVar RCV Id: RCV002387981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg451Pro
CA382533779
NM_001351834.2:c.1352G>C