Canonical Allele Identifier: PA2573226014
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1395937
ClinVar RCV Id: RCV001901292 RCV002482751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.His45Gln
CA371663023
NM_002485.5:c.135T>A
CA371663025
NM_002485.5:c.135T>G