Canonical Allele Identifier: PA1139705620
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 925449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ser88Phe
CA371662447
NM_002485.5:c.263C>T