Canonical Allele Identifier: PA2825335065
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 127009
ClinVar RCV Id: RCV000114875 RCV000115780 RCV000123203 RCV000212745 RCV000757930 RCV001358304 RCV000515275
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Leu339Ser
CA230729
NM_001024688.3:c.1016T>C