Canonical Allele Identifier: PA206705
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 142227
ClinVar RCV Id: RCV000131226 RCV000193311 RCV000168344 RCV000586867 RCV001354986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ser93Leu
CA206703
NM_002485.5:c.278C>T