Allele Registry

Canonical Allele Identifier: PA2825334257

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000115792

RCV000121616

RCV000123216

RCV000588621

ClinVar Variation:

127869

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Asp13Asn	CA160975 NM_001024688.3:c.37G>A