Allele Registry

Canonical Allele Identifier: PA658671383

Gene: NBN HGNC NCBI

ClinVar Allele:

458706

ClinVar RCV:

RCV000540870

ClinVar Variation:

461576

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Val22Phe	CA371663582 NM_002485.5:c.64G>T