Canonical Allele Identifier: PA658816399
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 530760
ClinVar RCV Id: RCV000636775 RCV001010019 RCV003465396 RCV003483697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Gln39Lys
CA181281098
NM_002485.5:c.115C>A