Canonical Allele Identifier: PA915956806
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 231708
ClinVar RCV Id: RCV000213516 RCV000764789 RCV000817138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asp39His
CA4802992
NM_001024688.3:c.115G>C