Canonical Allele Identifier: PA2825335812
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 848607
ClinVar RCV Id: RCV001052398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Lys604Glu
CA371676346
NM_001024688.3:c.1810A>G