Allele Registry

Canonical Allele Identifier: PA2825335070

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000572328

RCV001041861

ClinVar Variation:

483975

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Lys341Arg	CA371656233 NM_001024688.3:c.1022A>G