Canonical Allele Identifier: PA2580276336
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1965250
ClinVar RCV Id: RCV002726667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asn37Lys
CA371663196
NM_002485.5:c.111T>G
CA371663197
NM_002485.5:c.111T>A