Allele Registry

Canonical Allele Identifier: PA2825335356

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000536553

RCV000573249

ClinVar Variation:

461513

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Asn438Asp	CA181257926 NM_001024688.3:c.1312A>G