Canonical Allele Identifier: PA2499251030
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1063505
ClinVar RCV Id: RCV001373350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2258His
CA382555417
NM_001351834.2:c.6773T>A