Canonical Allele Identifier: PA2825335752
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1362892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asn584Lys
CA371676468
NM_001024688.3:c.1752C>G
CA371676469
NM_001024688.3:c.1752C>A