Canonical Allele Identifier: PA1139705349
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 837991
ClinVar RCV Id: RCV001039445 RCV003478669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Gly27Glu
CA371663426
NM_002485.5:c.80G>A