Allele Registry

Canonical Allele Identifier: PA2825334942

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000573508

RCV001341050

ClinVar Variation:

483991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Glu301Gln	CA371656492 NM_001024688.3:c.901G>C