Canonical Allele Identifier: PA915995869
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 825845
ClinVar RCV Id: RCV001024306 RCV003617888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Lys187Glu
CA371660176
NM_002485.5:c.559A>G