Allele Registry

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Canonical Allele Identifier: PA2825334255

Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 632917

ClinVar RCV Id: RCV000780523

ClinVar Variation Id: 834952

ClinVar RCV Id: RCV001035742

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Gly12Arg	CA371662416 NM_001024688.3:c.34G>C CA371662418 NM_001024688.3:c.34G>A