Canonical Allele Identifier: PA2825334229
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 490055
ClinVar RCV Id: RCV000580048 RCV001800798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Gln2Arg
CA4803015
NM_001024688.3:c.5A>G