Allele Registry

Canonical Allele Identifier: PA1139705658

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV001178737

ClinVar Variation:

920158

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Arg89Gly	CA371662446 NM_002485.5:c.265C>G