Allele Registry

Canonical Allele Identifier: PA658671985

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000573104

RCV000636736

RCV000985868

ClinVar Variation:

485916

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Met553Val	CA4802693 NM_002485.5:c.1657A>G