Canonical Allele Identifier: PA916034541
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482558
ClinVar RCV Id: RCV000567092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2637Arg
CA382561495
NM_001351834.2:c.7910A>G