Allele Registry

Canonical Allele Identifier: PA332809

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000123202

RCV000221417

RCV000484131

RCV000579707

RCV001264517

RCV003467093

ClinVar Variation:

136034

490042

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Ile35Thr	CA332807 NM_002485.5:c.104T>C CA658683519 NM_002485.5:c.102_104delinsAAC