Canonical Allele Identifier: PA2741897499
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2757667
ClinVar RCV Id: RCV003507150 RCV004369425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Val184Gly
CA371660209
NM_002485.5:c.551T>G