Canonical Allele Identifier: PA658816574
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 530719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asp295Val
CA371658217
NM_002485.5:c.884A>T