Canonical Allele Identifier: PA192431
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 185618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Gly274Arg
CA192429
NM_002485.5:c.820G>A
CA371658537
NM_002485.5:c.820G>C