Canonical Allele Identifier: PA915956886
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 127873
ClinVar RCV Id: RCV000115796 RCV000123218 RCV001030567 RCV000764786 RCV001549273 RCV003389690 RCV000587269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Arg87Cys
CA287937
NM_001024688.3:c.259C>T