Canonical Allele Identifier: PA2573226246
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1446553
ClinVar RCV Id: RCV001958530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Gln291His
CA371658274
NM_002485.5:c.873G>T
CA371658277
NM_002485.5:c.873G>C