Allele Registry

Canonical Allele Identifier: PA645465203

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000216738

RCV000533679

RCV001570359

RCV003475034

ClinVar Variation:

233580

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Ile35Met	CA4803056 NM_002485.5:c.105T>G